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RecruitingNCT07687576CAPTURE AMIUpdated Jul 10, 2026

Comparative Evaluation of Sustained meChanical AsPiration Thrombectomy and no Thrombus Modification for Pre-stent Thrombus bUrden Reduction in Patients With Acute Myocardial Infarction Study: the CAPTURE AMI Study

A Phase 2/3 interventional study of Sustained thrombectomy and Percutaneous Coronary Intervention in STEMI - ST Elevation Myocardial Infarction, sponsored by Oxford University Hospitals NHS Trust. Recruiting at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-07-10.

Sponsored by Oxford University Hospitals NHS Trust · Phase 2/3, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2026; still recruiting 4 months later.
Phase
Phase 2/3
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The CAPTURE AMI trial is an investigator-initiated, single-centre, two-arm, randomised controlled trial. Patients aged ≥ 18 years who present with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (pPCI) will be enrolled after angiographic evidence of a high thrombus burden (TIMI thrombus grade ≥ 4) and meeting the inclusion criteria laid out in section 9.2 will be 1:1 randomised to receive either standalone PCI (Arm 1) or adjunct sustained mechanical thrombectomy + PCI (Arm 2).

The CAPTURE AMI study will enrol specifically patients with:

A. Evidence of high thrombus burden on coronary angiography (TIMI thrombus grade ≥ 4) B. Culprit in an artery with a diameter of 3.0 mm or more. The trial is designed to evaluate the efficacy of sustained mechanical thrombectomy versus standalone PCI in patients with a large thrombus burden assessed angiographically, with a pre-stent thrombus burden (%) as the primary imaging endpoint.

02

Conditions studied

  • STEMI - ST Elevation Myocardial Infarction

Keywords

  • Thrombus
  • Thrombectomy
  • Optical Coherence Tomography
  • Microvascular Injury
03

In context

ST Elevation Myocardial Infarction

850 studies on the registry are indexed under ST Elevation Myocardial Infarction; 197 are open to participants now.

This study's planned enrollment of 60 is below the median of 194 across 527 interventional studies indexed under ST Elevation Myocardial Infarction.

Browse ST Elevation Myocardial Infarction studies →

Lead sponsor

Oxford University Hospitals NHS Trust is the lead sponsor of 94 studies on the registry; 7 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Primary PCI patient with ST elevation myocardial infarction
  • Angiographic criteria:

    • TIMI 0/1 flow at presentation
    • Angiographic thrombus score ≥ 4
    • Vessel diameter at site of occlusion ≥ 3.0mm (determined by coronary angiography)

Exclusion criteria

Exclusion Criteria:

  • Female participant who is pregnant or lactating
  • Unconscious at presentation
  • Late STEMI presentation (symptoms onset to wire time > 12 h)
  • Clinically/haemodynamically unstable patients
  • Known diagnosis of severe renal disease (CKD stage 4-5)
  • Suspected spontaneous coronary artery dissection
  • Previous CABG
  • Previous history on STEMI in the same culprit territory
  • Known moderate-severe anaemia ( \< 9)
Terms in these criteria, in plain language(1)

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.

Hemoglobin (Hb)

The protein in red blood cells that carries oxygen. A low level is anaemia, which can cause tiredness and breathlessness. Measured in g/dL or g/L (9 g/dL is 90 g/L).

05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Standalone PCI

    Standalone OCT guided PCI

    Procedure: Percutaneous Coronary Intervention

  • Experimental
    PCI & Sustained thrombectomy

    OCT guided PCI \& Sustained Thrombectomy

    Device: Sustained thrombectomy · Procedure: Percutaneous Coronary Intervention

Interventions

  • DeviceSustained thrombectomy

    Sustained thrombectomy with the Indigo® System CAT™ RX aspiration catheter

  • ProcedurePercutaneous Coronary Intervention

    Optical Coherence Tomography guided Percutaneous Coronary Intervention

06

What researchers measure

Primary outcomes

  1. Pre stent Thrombus Burden

    Pre stent Thrombus Burden (thrombus volume/lumen volume) evaluated by Optical Coherence Tomography

    Time frame: Pre stent implantation (Periprocedural)

Other outcomes

  1. Clinical Outcomes

    Rate of major adverse cardiac and cerebrovascular events (MACCE)

    Time frame: In hospital (Pre-discharge), 30 days & 6 months

  2. Efficacy of thrombus burden reduction

    Thrombus volume (mm3) by Optical Coherence Tomography

    Time frame: Pre stent implantation (Periprocedural)

  3. Efficacy of thrombus burden reduction

    Thrombus area, flow area (mm2) by Optical Coherence Tomography

    Time frame: Pre stent Implantation (Periprocedural)

  4. Efficacy of thromboatheroma reduction

    Thromboatheroma volume (mm3), flow volume (mm3) by Optical Coherence Tomography

    Time frame: Post stent implantation (Periprocedural)

  5. Efficacy of target vessel reperfusion

    Coronary Flow Reserve (CFR) and Index of Microcirculatory Resistance (IMR) assessment in target vessel

    Time frame: Post stent Implantation (Periprocedural)

  6. Efficacy of stent implantation

    Stent expansion \& apposition by Optical Coherence Tomography

    Time frame: Post stent implantation (Periprocedural)

07

Study locations

1 of 1 sites recruiting
08

References and documents

Publications

  • Kotronias RA, Walsh JL, Andreaggi S, Portolan L, Maino A, Marin F, Chai J, Sobirov I, Sheikh M, Cahill TJ, Lucking AJ, Costello M, Fraile Moreno E, Haridas V, Shaji A, Garcia-Garcia HM, Channon KM, Banning AP, Langrish JP, De Maria GL; OxAMI and RETRIEVE AMI Investigators. Stent-Retriever Thrombectomy in STEMI With Large Thrombus Burden: The RETRIEVE AMI Randomized Trial. JACC Adv. 2025 Jul;4(7):101893. doi: 10.1016/j.jacadv.2025.101893. Epub 2025 Jun 23. PubMed 40555011 ↗
  • Walsh JL, Kotronias RA, Banning AP, De Maria GL. Interventional thrombus modification in STEMI. Nat Rev Cardiol. 2024 Jul;21(7):435-436. doi: 10.1038/s41569-024-01020-2. No abstract available. PubMed 38565957 ↗
  • Kotronias RA, Marin F, Emfietzoglou M, Langrish JP, Lucking AJ, Channon KM, Banning AP, De Maria GL. Rationale and Design of a Randomized Controlled Pilot Trial to Assess Stent Retriever Thrombectomy for Thrombus Burden Reduction in Patients with Acute Myocardial Infarction: The RETRIEVE-AMI Study. Cardiovasc Revasc Med. 2023 Jul;52:75-85. doi: 10.1016/j.carrev.2023.02.012. Epub 2023 Mar 6. PubMed 36894360 ↗

Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jul 2026 (actual). Primary completion is estimated for Jul 2027, 12 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 25, 2026
First posted
Jul 7, 2026
StartActual
Jul 8, 2026
Primary completionEst.
Jul 8, 2027
CompletionEst.
Jan 8, 2028
Last update
Jul 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jul 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07687576
Lead sponsor
Oxford University Hospitals NHS Trust
Responsible party
Giovanni Luigi De Maria (Primary Investigator, Oxford University Hospitals NHS Trust) — Principal investigator
First posted
Jul 7, 2026
Start date
Jul 8, 2026
Primary completion
Jul 8, 2027 (estimated)
Completion
Jan 8, 2028 (estimated)
Last update
Jul 10, 2026

Study contacts

Giovanni Luigi De Maria, MD
Contact
GiovanniLuigi.DeMaria@ouh.nhs.uk
+44 18655 528364

Oversight

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

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