ClinicalTrials.gg
RecruitingNCT06689839SHIELDUpdated Nov 6, 2026

Trial of the F2 Filter and Delivery System for Embolic Protection During TAVR

An interventional study of F2 Filter and Delivery System and Transcatheter Aortic Valve Replacement (TAVR) in Aortic Stenosis Treated With TAVI and Aortic Diseases, sponsored by EnCompass Technologies, Inc.. Recruiting at 10 sites in 2 countries. Open to participants aged 21 Years to 90 Years. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by EnCompass Technologies, Inc. · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2025; still recruiting 1 year 2 months later.
Updated Nov 6, 2026Sponsor changedEligibility revised+5 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
500
Allocation
Randomized
Ages
21 Years to 90 Years
Sex
All
01

Study summary

The objective of this pivotal study is to compare the safety and effectiveness of the F2 CPC (Treatment group) to a Control group (no embolic protection) in participants undergoing transfemoral (TF) TAVR with commercially available devices.

Read the detailed description

The study is designed to demonstrate that the F2 CPC performs in a consistent manner as the control group in terms of safety, and the F2 Cerebral Protection Catheter (CPC) will be superior in performance when compared to the control group in terms of effectiveness in patients undergoing Transcatheter Aortic Valve Replacement (TF TAVR).

02

Conditions studied

  • Aortic Stenosis Treated With TAVI
  • Aortic Diseases

Keywords

  • Embolic Protection
  • Transcatheter Aortic Valve Replacement
  • TAVR
  • Aortic Valve Stenosis
  • Aortic Valve Diseases
03

In context

Aortic Diseases

108 studies on the registry are indexed under Aortic Diseases; 43 are open to participants now.

This study's planned enrollment of 500 is above the median of 90 across 42 interventional studies indexed under Aortic Diseases.

Browse Aortic Diseases studies →

Lead sponsor

EnCompass Technologies, Inc. is the lead sponsor of 4 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

The criteria were revised on the registry on Oct 26, 2026. See what changed

Ages eligible
21 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Key Inclusion Criteria:

  1. Age ≥ 21 and ≤ 90 years
  2. Patient meets the established criteria and indications for commercially available TAVR (e.g., balloon expandable SAPIEN valve platform, self-expanding CoreValve platform, or Navitor TAVI System) via transfemoral access and is scheduled to undergo TAVR per their treating physician.
  3. Patient is willing and able to comply with protocol-specified follow-up evaluations.
  4. Patient is able and willing to provide written

Key Exclusion Criteria:

General Exclusion Criteria:

Participants are not eligible for the study if any of the following criteria are present:

General Exclusion Criteria:

  1. Requires an urgent or emergent TAVR procedure.
  2. Any interventional cardiovascular procedure performed within 30 days prior to TAVR procedure (e.g., pacemaker placement, BAV, PCI) or planned within 30 days post-TAVR procedure.
  3. Current or planned participation in any device/biopharma study during the duration of this study protocol.
  4. Diagnostic cardiac catheterization within 10 days prior to TAVR procedure (Note: unplanned diagnostic catheterization is allowed during TAVR procedure, but must be performed prior to insertion of the investigational device into the vasculature).
  5. Concomitant non-valvular intervention, vascular intervention, or leaflet modification is planned at time of TAVR procedure. (Note: balloon aortic valvuloplasty during TAVR procedure is permitted).
  6. Evidence of an acute myocardial infarction within 3 months prior to TAVR procedure.
  7. Prior prosthetic heart valve in any position.
  8. Known intracardiac thrombus.
  9. Active infection or endocarditis.
  10. Severe allergy or known or to aspirin, heparin/bivalirudin, clopidogrel, nitinol, stainless steel alloy, nickel-titanium and/or contrast sensitivity that cannot be adequately pre-medicated.
  11. Presence or history of bleeding diathesis or coagulopathy.
  12. Contraindicated for anti- and/or anticoagulant therapy.
  13. Refuses blood transfusion.
  14. Active peptic ulcer or history of upper gastrointestinal (GI) bleeding within the 3 months prior to TAVR procedure.
  15. Renal insufficiency (creatinine > 2.5 mg/dL or \< 30) and/or renal replacement therapy at the time of screening.
  16. Hepatic failure ( class C).
  17. Presenting with cardiogenic shock or requiring vasopressor or inotropic support, or with severe hypotension (systolic blood pressure \< 90 mm Hg) at the time of randomization.
  18. Severe ventricular dysfunction with (LVEF) \< 30%.
  19. Females who are pregnant or nursing or plan to become pregnant during their participation in the study. Female participants of must have a negative pregnancy test at screening.
  20. Any other condition that in the opinion of the investigator precludes study participation or poses a significant hazard to the patient.

Neurological Exclusion Criteria:

  1. Modified Rankin Scale (mRS) ≥ 2 at screening.
  2. Cerebrovascular event including within 6 months of the procedure.
  3. Active major psychiatric disease, known mental or physical illness or known history of substance abuse that may cause non-compliance with the protocol or confound the data interpretation.
  4. Severe visual, auditory, or learning impairment.
  5. Neurodegenerative or other progressive neurological disease or history of significant head trauma followed by persistent neurologic defaults or known structural brain abnormalities.

Note: use of general anesthesia during TAVR may affect neurocognitive function shortly after the procedure. While not an exclusion criterion, it is recommended that general anesthesia not be used, if possible.

Magnetic Resonance Imaging Exclusion Criteria:

  1. (BMI) precluding imaging in scanner.
  2. Contraindications to MRI (participants with MR unsafe implants including implantable temporary or permanent pacemaker or defibrillator, metal implants in field of view, metallic fragments, clips, or devices in the brain or eye before TAVR procedure).
  3. High risk of complete AV block after TAVR, with the need of permanent pacemaker (e.g., patients with pre-existing bifascicular block or complete right bundle branch block plus any degree of AV block).
  4. Claustrophobia precluding MRI scanning.

Anatomical and CT Exclusion Criteria:

  1. Severe peripheral arterial, abdominal aortic, or thoracic aortic disease that precludes delivery sheath, vascular access or filter deployment.
  2. Presence of cardiovascular implant in aorta and/or peripheral access vessels (e.g., thoracic endovascular aortic repair [TEVAR]/endovascular abdominal aortic aneurysm repair [EVAR], iliac/superficial femoral artery [SFA] stent).
  3. Access vessels with excessive tortuosity or complex anatomy that would likely necessitate a surgical cutdown approach (e.g., distance from skin to vessel is extensive).
  4. Aortic arch, which is heavily calcified, severely atheromatous, or severely tortuous.
  5. Ascending aortic diameter less than 18 mm or greater than 38 mm measured 6 to 8 cm from the annulus.
  6. Transverse aortic arch diameter less than 18 mm or greater than 27 mm when measured immediately proximal to the ostium of the left subclavian artery.
Terms in these criteria, in plain language(11)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

Child-Pugh class

A score of how well the liver works in people with liver disease such as cirrhosis: class A is mild, B moderate and C severe.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
500 participants (estimated)

Study arms

  • Experimental
    F2 Filter and Delivery System

    The F2 Cerebral Embolic Protection System will be used during your Transcatheter Aortic Valve Replacement procedure.

    Device: F2 Filter and Delivery System · Procedure: Transcatheter Aortic Valve Replacement (TAVR)

  • Active comparator
    No embolic protection device

    No embolic protection device will be used during your Transcatheter Aortic Valve Replacement procedure.

    Procedure: Transcatheter Aortic Valve Replacement (TAVR)

Interventions

  • DeviceF2 Filter and Delivery System

    Use of the F2 Filter and Delivery System in conjunction with a Transcatheter Aortic Valve Replacement (TAVR) procedure

  • ProcedureTranscatheter Aortic Valve Replacement (TAVR)

    Transcatheter Aortic Valve Replacement (TAVR) with commercially available Transcatheter Aortic Valve Replacement (TAVR) device

06

What researchers measure

Primary outcomes

  1. Ability of the F2 CPC to provide neuroprotection during a TF TAVR procedure

    Determined by pair-wise comparisons among participants in the eITT population (Finkelstein-Schoenfeld \[FS\] method) according to the following prespecified hierarchy of adverse outcomes: * Ischemic stroke (disabling or non-disabling); evaluated through 72 hours post-procedure * Total new lesion volume by DW-MRI; evaluated at 8-72 hours post-procedure by an independent MRI Core Laboratory.

    Time frame: 8 to 72 hours post procedure

  2. Major Adverse Events (MAE)

    Defined as the composite of the following components at 30 days: * All-cause mortality * All stroke (disabling and non-disabling) * Acute kidney injury (Stage 3)

    Time frame: 30 days post procedure

Secondary outcomes

  1. Combined Safety and Efficacy - VARC-2

    All-cause mortality; all stroke (disabling and non-disabling) and transient ischemic attack (TIA); acute kidney injury (stage 2 or 3, including renal replacement therapy)

    Time frame: Discharge or Day 5-10, whichever comes first

  2. Neurological events (VARC-2 and NeuroARC)

    Stroke (subclassified as ischemic, hemorrhagic, or undetermined, and as disabling or non-disabling); TIA

    Time frame: Discharge or Day 5-10, whichever comes first; Day 30

  3. Incidence of acute kidney injury (AKIN)

    Subclassified as stage 1, 2, or 3 Acute Kidney Injury (VARC-2)

    Time frame: Discharge or Day 5-10, whichever comes first; Day 30

  4. Incidence of major vascular complications (VARC-3)

    Time frame: Discharge or Day 5-10, whichever comes first; Day 30

  5. Bleeding

    Incidence of life-threatening or disabling bleeding and major bleeding (VARC-2) - life-threatening or disabling bleeding; major bleeding

    Time frame: Discharge or Day 5-10, whichever comes first; Day 30

  6. Major adverse embolic events (MAEE)

    Incidence of the composite of all stroke (disabling or non-disabling) and transient ischemic attack (TIA), and Acute Kidney Injury Stage 2 or 3 (including renal replacement therapy), and systemic embolization

    Time frame: Discharge or Day 5-10

  7. Total volume of new lesions by DW-MRI

    Assessed by an independent MRI Core Laboratory

    Time frame: 8-72 hours post-procedure

Other outcomes

  1. NIHSS

    NIHSS worsening (increase of 2 or more from baseline)

    Time frame: Discharge or Day 5-10, whichever comes first; Day 30

  2. MoCA

    MoCA worsening (decrease of 2 or more from baseline)

    Time frame: Discharge or Day 5-10, whichever comes first; Day 30

  3. Number of new lesions by DW-MRI

    Assessed by an independent MRI Core Laboratory

    Time frame: 8-72 hours post-procedure

  4. Average size of new lesions by DW-MRI

    Assessed by an independent MRI Core Laboratory

    Time frame: 8-72 hours post-procedure

  5. Largest per-subject single new lesion by DW-MRI

    Assessed by an independent MRI Core Laboratory

    Time frame: 8-72 hours post-procedure

07

Study locations

6 of 10 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

3 registry updates since Sep 25, 2026
Sites
2 sites added, 2 sites removed
Show 2 added (2 United States)
  • St. Vincent Hospital · Indianapolis, United States
  • St. Vincent Hospital · Indianappolis, United States
Show 2 removed
  • St. Vincent Hospital · Indianappolis, United States
  • St. Vincent Hospital · Indianapolis, United States
across 2 updates, Oct 26, 2026 – Nov 6, 2026
Eligibility
Minimum age 50 Years→21 Years; Maximum age none→90 Years; 12 criteria edited, 16 added, 4 removed
What changed in the criteria
  • EditedAge ≥ 5021 and ≤ 90 years.
  • EditedPatient meets the established criteria and indications for commercially available TAVR (e.g., balloon expandable SAPIEN valve platform, self-expanding CoreValve platform, or Navitor TAVI System) via transfemoral access and is scheduled to undergo TAVR per their treating physician.
  • RemovedPatient meets all criteria for use of control device (Sentinel device, per IFU).
  • AddedParticipants are not eligible for the study if any of the following criteria are present:
  • AddedGeneral Exclusion Criteria:
  • EditedPatient requiresRequires an urgent or emergent TAVR procedure.
  • EditedAny interventional cardiovascular procedure performed within 30 days prior to TAVR procedure (e.g., pacemaker placement, BAV, PCI) or planned within 30 days post-TAVR procedure.
  • RemovedDiagnostic cardiac catheterization within 10 days prior to TAVR procedure.
  • AddedCurrent or planned participation in any investigational device/biopharma study during the duration of this study protocol.
  • AddedDiagnostic cardiac catheterization within 10 days prior to TAVR procedure (Note: unplanned diagnostic catheterization is allowed during TAVR procedure, but must be performed prior to insertion of the investigational device into the vasculature).
  • AddedConcomitant non-valvular intervention, vascular intervention, or leaflet modification is planned at time of TAVR procedure. (Note: balloon aortic valvuloplasty during TAVR procedure is permitted).
  • AddedSevere allergy or known hypersensitivity or contraindication to aspirin, heparin/bivalirudin, clopidogrel, nitinol, stainless steel alloy, nickel-titanium and/or contrast sensitivity that cannot be adequately pre-medicated.
  • AddedPresence or history of bleeding diathesis or coagulopathy.
  • EditedPatient is contraindicatedContraindicated for anti-platelet and/or anticoagulant therapy.
  • EditedPatient refusesRefuses blood transfusion.
  • AddedActive peptic ulcer or history of upper gastrointestinal (GI) bleeding within the 3 months prior to TAVR procedure.
  • EditedPatients with hepaticHepatic failure (Child-Pugh class C).
  • AddedPresenting with cardiogenic shock or requiring vasopressor or inotropic support, or with severe hypotension (systolic blood pressure < 90 mm Hg) at the time of randomization.
  • EditedFemales who are pregnant or nursing or plan to become pregnant during their participation in the study. Female participants of child-bearing potential must have a negative pregnancy test at screening.
  • AddedAny other condition that in the opinion of the investigator precludes study participation or poses a significant hazard to the patient.
  • EditedPatient has activeActive major psychiatric disease, known mental or physical illness or known history of substance abuse that may cause non-compliance with the protocol or confound the data interpretation.
  • EditedPatient has severeSevere visual, auditory, or learning impairment.
  • EditedPatient has neurodegenerativeNeurodegenerative or other progressive neurological disease or history of significant head trauma followed by persistent neurologic defaults or known structural brain abnormalities.
  • AddedNote: use of general anesthesia during TAVR may affect neurocognitive function shortly after the procedure. While not an exclusion criterion, it is recommended that general anesthesia not be used, if possible.
  • AddedBody Mass Index (BMI) precluding imaging in scanner.
  • EditedHigh risk of complete AV block after TAVR, with the need of permanent pacemaker (e.g., patients with pre-existing bifascicular block or complete right bundle branch block plus any degree of AV block).
  • RemovedPresence of cardiovascular implant in aorta and/or peripheral access vessels.
  • RemovedAccess vessels with excessive tortuosity.
  • AddedPresence of cardiovascular implant in aorta and/or peripheral access vessels (e.g., thoracic endovascular aortic repair [TEVAR]/endovascular abdominal aortic aneurysm repair [EVAR], iliac/superficial femoral artery [SFA] stent).
  • AddedAccess vessels with excessive tortuosity or complex anatomy that would likely necessitate a surgical cutdown approach (e.g., distance from skin to vessel is extensive).
  • AddedAscending aortic diameter less than 18 mm or greater than 38 mm measured 6 to 8 cm from the annulus.
  • AddedTransverse aortic arch diameter less than 18 mm or greater than 27 mm when measured immediately proximal to the ostium of the left subclavian artery.
Oct 26, 2026
Interventions
Arm changed Either the Sentinel Cerebral Protection System or no embolic protection device→No embolic protection device
Oct 26, 2026
Primary outcomes
2 edited
What changed in the outcomes
  • EditedMajor Adverse Cardiac and Cerebrovascular Events (MACCEMAE)Time frame: 30 days post procedure
  • ChangedBefore Total New Lesion VolumeNow Ability of the F2 CPC to provide neuroprotection during a TF TAVR procedureTime frame: 8-72 hours post procedure → 8 to 72 hours post procedure
Oct 26, 2026
Secondary outcomes
12 added, 14 removed
What changed in the outcomes
  • AddedCombined Safety and Efficacy - VARC-2Time frame: Discharge or Day 5-10, whichever comes first
  • AddedNeurological events (VARC-2 and NeuroARC)Time frame: Discharge or Day 5-10, whichever comes first; Day 30
  • AddedIncidence of acute kidney injury (AKIN)Time frame: Discharge or Day 5-10, whichever comes first; Day 30
  • AddedIncidence of major vascular complications (VARC-3)Time frame: Discharge or Day 5-10, whichever comes first; Day 30
  • AddedBleedingTime frame: Discharge or Day 5-10, whichever comes first; Day 30
  • AddedMajor adverse embolic events (MAEE)Time frame: Discharge or Day 5-10
  • AddedTotal volume of new lesions by DW-MRITime frame: 8-72 hours post-procedure
  • RemovedStrokeTime frame: 30 days post procedure
  • Addedother outcomeNIHSSTime frame: Discharge or Day 5-10, whichever comes first; Day 30
  • Addedother outcomeMoCATime frame: Discharge or Day 5-10, whichever comes first; Day 30
  • Addedother outcomeNumber of new lesions by DW-MRITime frame: 8-72 hours post-procedure
  • Addedother outcomeAverage size of new lesions by DW-MRITime frame: 8-72 hours post-procedure
  • Addedother outcomeLargest per-subject single new lesion by DW-MRITime frame: 8-72 hours post-procedure
  • Removedother outcomePerformanceTime frame: During procedure
  • Removedother outcomeMortality & Stroke RatesTime frame: 30 days post procedure
  • Removedother outcomeFreedom from LesionsTime frame: 8-72 hours post procedure
  • Removedother outcomeAverage Lesion SizeTime frame: 8-72 hours post procedure
  • Removedother outcomeNeurological Outcomes-National Institute of Health Stroke Scale (NIHSS)Time frame: 30 days post procedure
  • Removedother outcomeNeurological Outcomes-Montreal Cognitive Assessment (MoCA)Time frame: 30 days post procedure
  • Removedother outcomeNeurological Outcomes-Modified Rankin Scale (MRS)Time frame: 30 days post procedure
  • Removedother outcomeMajor Vascular Complication & BleedingTime frame: During procedure
  • Removedother outcomeHospital ReadmissionsTime frame: 30 days post procedure
  • Removedother outcomeIndex Hospital Length of Stay (LOS)Time frame: Through 30 days
  • Removedother outcomeIndex Hospitalization ICU Length of Stay (LOS)Time frame: Through 30 days
  • Removedother outcomeKansas City Cardiomyopathy Questionnaire (KCCQ)Time frame: 30 days post procedure
  • Removedother outcomeShort Form (SF-12) QuestionnaireTime frame: 30 days post procedure
Oct 26, 2026
Contact
Study contact changed: k•••@encompassf2.com · •••2726→s•••@encompassf2.com · •••8652. See the current contact
Oct 26, 2026
Site contacts
Changed at 1 site. See the sites
Show the site
  • Monash Health Public · Clayton, AustraliaContact T•••@monashhealth.org→m•••@monashhealth.org
Nov 6, 2026
Sponsor
Collaborators added: DP Clinical, Inc.·Avania Pty Ltd; collaborators removed: Avania·Insight Medical Consulting
across 3 updates, Oct 26, 2026 – Nov 6, 2026
Show all 3 updates
  1. Nov 6, 2026
    1 site added, 1 site removed
    Show site
    • St. Vincent Hospital · Indianappolis, United States
    Show 1 removed
    • St. Vincent Hospital · Indianapolis, United States
    Sponsor Collaborators added: Avania Pty Ltd; collaborators removed: Avania AUS
    Site contacts Changed at 1 site. See the sites
    Show the site
    • Monash Health Public · Clayton, AustraliaContact T•••@monashhealth.org→m•••@monashhealth.org
  2. Oct 30, 2026
    Sponsor Collaborators added: Avania AUS
  3. Oct 26, 2026
    1 site added, 1 site removed
    Show site
    • St. Vincent Hospital · Indianapolis, United States
    Show 1 removed
    • St. Vincent Hospital · Indianappolis, United States
    Eligibility Minimum age 50 Years→21 Years; Maximum age none→90 Years; 12 criteria edited, 16 added, 4 removed
    What changed in the criteria
    • EditedAge ≥ 5021 and ≤ 90 years.
    • EditedPatient meets the established criteria and indications for commercially available TAVR (e.g., balloon expandable SAPIEN valve platform, self-expanding CoreValve platform, or Navitor TAVI System) via transfemoral access and is scheduled to undergo TAVR per their treating physician.
    • RemovedPatient meets all criteria for use of control device (Sentinel device, per IFU).
    • AddedParticipants are not eligible for the study if any of the following criteria are present:
    • AddedGeneral Exclusion Criteria:
    • EditedPatient requiresRequires an urgent or emergent TAVR procedure.
    • EditedAny interventional cardiovascular procedure performed within 30 days prior to TAVR procedure (e.g., pacemaker placement, BAV, PCI) or planned within 30 days post-TAVR procedure.
    • RemovedDiagnostic cardiac catheterization within 10 days prior to TAVR procedure.
    • AddedCurrent or planned participation in any investigational device/biopharma study during the duration of this study protocol.
    • AddedDiagnostic cardiac catheterization within 10 days prior to TAVR procedure (Note: unplanned diagnostic catheterization is allowed during TAVR procedure, but must be performed prior to insertion of the investigational device into the vasculature).
    • AddedConcomitant non-valvular intervention, vascular intervention, or leaflet modification is planned at time of TAVR procedure. (Note: balloon aortic valvuloplasty during TAVR procedure is permitted).
    • AddedSevere allergy or known hypersensitivity or contraindication to aspirin, heparin/bivalirudin, clopidogrel, nitinol, stainless steel alloy, nickel-titanium and/or contrast sensitivity that cannot be adequately pre-medicated.
    • AddedPresence or history of bleeding diathesis or coagulopathy.
    • EditedPatient is contraindicatedContraindicated for anti-platelet and/or anticoagulant therapy.
    • EditedPatient refusesRefuses blood transfusion.
    • AddedActive peptic ulcer or history of upper gastrointestinal (GI) bleeding within the 3 months prior to TAVR procedure.
    • EditedPatients with hepaticHepatic failure (Child-Pugh class C).
    • AddedPresenting with cardiogenic shock or requiring vasopressor or inotropic support, or with severe hypotension (systolic blood pressure < 90 mm Hg) at the time of randomization.
    • EditedFemales who are pregnant or nursing or plan to become pregnant during their participation in the study. Female participants of child-bearing potential must have a negative pregnancy test at screening.
    • AddedAny other condition that in the opinion of the investigator precludes study participation or poses a significant hazard to the patient.
    • EditedPatient has activeActive major psychiatric disease, known mental or physical illness or known history of substance abuse that may cause non-compliance with the protocol or confound the data interpretation.
    • EditedPatient has severeSevere visual, auditory, or learning impairment.
    • EditedPatient has neurodegenerativeNeurodegenerative or other progressive neurological disease or history of significant head trauma followed by persistent neurologic defaults or known structural brain abnormalities.
    • AddedNote: use of general anesthesia during TAVR may affect neurocognitive function shortly after the procedure. While not an exclusion criterion, it is recommended that general anesthesia not be used, if possible.
    • AddedBody Mass Index (BMI) precluding imaging in scanner.
    • EditedHigh risk of complete AV block after TAVR, with the need of permanent pacemaker (e.g., patients with pre-existing bifascicular block or complete right bundle branch block plus any degree of AV block).
    • RemovedPresence of cardiovascular implant in aorta and/or peripheral access vessels.
    • RemovedAccess vessels with excessive tortuosity.
    • AddedPresence of cardiovascular implant in aorta and/or peripheral access vessels (e.g., thoracic endovascular aortic repair [TEVAR]/endovascular abdominal aortic aneurysm repair [EVAR], iliac/superficial femoral artery [SFA] stent).
    • AddedAccess vessels with excessive tortuosity or complex anatomy that would likely necessitate a surgical cutdown approach (e.g., distance from skin to vessel is extensive).
    • AddedAscending aortic diameter less than 18 mm or greater than 38 mm measured 6 to 8 cm from the annulus.
    • AddedTransverse aortic arch diameter less than 18 mm or greater than 27 mm when measured immediately proximal to the ostium of the left subclavian artery.
    Primary outcomes 2 edited
    What changed in the outcomes
    • EditedMajor Adverse Cardiac and Cerebrovascular Events (MACCEMAE)Time frame: 30 days post procedure
    • ChangedBefore Total New Lesion VolumeNow Ability of the F2 CPC to provide neuroprotection during a TF TAVR procedureTime frame: 8-72 hours post procedure → 8 to 72 hours post procedure
    Secondary outcomes 12 added, 14 removed
    What changed in the outcomes
    • AddedCombined Safety and Efficacy - VARC-2Time frame: Discharge or Day 5-10, whichever comes first
    • AddedNeurological events (VARC-2 and NeuroARC)Time frame: Discharge or Day 5-10, whichever comes first; Day 30
    • AddedIncidence of acute kidney injury (AKIN)Time frame: Discharge or Day 5-10, whichever comes first; Day 30
    • AddedIncidence of major vascular complications (VARC-3)Time frame: Discharge or Day 5-10, whichever comes first; Day 30
    • AddedBleedingTime frame: Discharge or Day 5-10, whichever comes first; Day 30
    • AddedMajor adverse embolic events (MAEE)Time frame: Discharge or Day 5-10
    • AddedTotal volume of new lesions by DW-MRITime frame: 8-72 hours post-procedure
    • RemovedStrokeTime frame: 30 days post procedure
    • Addedother outcomeNIHSSTime frame: Discharge or Day 5-10, whichever comes first; Day 30
    • Addedother outcomeMoCATime frame: Discharge or Day 5-10, whichever comes first; Day 30
    • Addedother outcomeNumber of new lesions by DW-MRITime frame: 8-72 hours post-procedure
    • Addedother outcomeAverage size of new lesions by DW-MRITime frame: 8-72 hours post-procedure
    • Addedother outcomeLargest per-subject single new lesion by DW-MRITime frame: 8-72 hours post-procedure
    • Removedother outcomePerformanceTime frame: During procedure
    • Removedother outcomeMortality & Stroke RatesTime frame: 30 days post procedure
    • Removedother outcomeFreedom from LesionsTime frame: 8-72 hours post procedure
    • Removedother outcomeAverage Lesion SizeTime frame: 8-72 hours post procedure
    • Removedother outcomeNeurological Outcomes-National Institute of Health Stroke Scale (NIHSS)Time frame: 30 days post procedure
    • Removedother outcomeNeurological Outcomes-Montreal Cognitive Assessment (MoCA)Time frame: 30 days post procedure
    • Removedother outcomeNeurological Outcomes-Modified Rankin Scale (MRS)Time frame: 30 days post procedure
    • Removedother outcomeMajor Vascular Complication & BleedingTime frame: During procedure
    • Removedother outcomeHospital ReadmissionsTime frame: 30 days post procedure
    • Removedother outcomeIndex Hospital Length of Stay (LOS)Time frame: Through 30 days
    • Removedother outcomeIndex Hospitalization ICU Length of Stay (LOS)Time frame: Through 30 days
    • Removedother outcomeKansas City Cardiomyopathy Questionnaire (KCCQ)Time frame: 30 days post procedure
    • Removedother outcomeShort Form (SF-12) QuestionnaireTime frame: 30 days post procedure
    Interventions Arm changed Either the Sentinel Cerebral Protection System or no embolic protection device→No embolic protection device
    Sponsor Collaborators added: DP Clinical, Inc.; collaborators removed: Avania·Insight Medical Consulting
    Contact Study contact changed: k•••@encompassf2.com · •••2726→s•••@encompassf2.com · •••8652. See the current contact
    + 3 other changes: identifiers, description and design details

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT06689839
Lead sponsor
EnCompass Technologies, Inc.
Collaborators
DP Clinical, Inc., Avania Pty Ltd
Responsible party
Sponsor
First posted
Nov 15, 2024
Start date
Sep 9, 2025
Primary completion
Dec 2026 (estimated)
Completion
Jan 2027 (estimated)
Last update
Nov 6, 2026

Study contacts

Sandra Show
Contact
sshow@encompassf2.com
7142928652

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion