ClinicalTrials.gg
Not yet recruitingNCT07602790EMBRACEUpdated May 22, 2026

Expand Management of Blood Pressure With Renal Denervation in Patients Undergoing Staged PCI for Advanced Coronary Artery diseasE

An interventional study of Renal denervation in Multivessel Coronary Artery Disease and Hypertension Resistant to Conventional Therapy, sponsored by Ceric Sàrl. Not yet recruiting. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2026-05-22.

Sponsored by Ceric Sàrl · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
1,000
Allocation
Randomized
Ages
21 Years and older
Sex
All
01

Study summary

EMBRACE is a randomized, controlled, multicenter clinical study evaluating the effect of renal denervation on clinical adverse events in hypertensive patients undergoing staged percutaneous coronary intervention (PCI) for multivessel coronary artery disease.

Read the detailed description

Hypertension remains one of the most important modifiable risk factors for cardiovascular morbidity and mortality worldwide. Despite the availability of multiple antihypertensive drug classes and evidence based treatment strategies, a substantial proportion of patients continue to have inadequately controlled blood pressure. Poor blood pressure control is particularly common among patients with multivessel coronary artery disease and is associated with increased adverse cardiovascular outcomes, including myocardial infarction, stroke, heart failure, progression of renal dysfunction, and increased mortality.

Renal sympathetic nerve activity plays a central role in the pathophysiology of hypertension through modulation of renal blood flow, sodium and water retention, renin release, and systemic sympathetic tone. Renal denervation is a catheter based procedure designed to disrupt renal sympathetic afferent and efferent nerves by delivering energy to the renal artery wall. Multiple randomized clinical studies have demonstrated that renal denervation can reduce blood pressure in patients with uncontrolled hypertension, with sustained effects during follow up and an acceptable safety profile when performed using contemporary devices and techniques.

Patients with multivessel coronary artery disease undergoing percutaneous coronary intervention represent a particularly relevant population in which blood pressure control is of critical importance. In many cases, coronary revascularization is performed as a staged procedure, with an initial index PCI followed by a planned staged PCI to complete revascularization of remaining significant coronary lesions. This staged approach allows for optimization of patient safety and procedural efficiency, particularly in patients with complex coronary anatomy or a high ischemic burden.

The EMBRACE study is designed to evaluate the benefit of renal denervation in improving clinical outcomes in patients with multivessel coronary artery disease undergoing staged percutaneous coronary intervention. This study is a prospective, randomized, controlled, multicenter clinical investigation. Eligible patients are adults with multivessel coronary artery disease undergoing staged PCI who have hypertension defined as persistent elevation of office systolic blood pressure despite treatment with two or more antihypertensive medications. Following confirmation of eligibility and completion of the index PCI, patients who remain eligible prior to the planned staged PCI are randomized in a 1:1 allocation ratio to receive renal denervation in addition to standard care or standard care alone.

Renal denervation is performed using a commercially available catheter based renal denervation system in accordance with the manufacturer's instructions for use. The procedure is carried out via standard endovascular access and is performed either during the staged PCI procedure or as a standalone catheter based intervention, depending on procedural planning and investigator judgment. All patients continue to receive guideline directed medical therapy for hypertension and coronary artery disease throughout the study.

Patients randomized to the control group undergo staged PCI and continue standard medical therapy without renal denervation. Antihypertensive medications are managed according to routine clinical practice, with adjustments permitted at the discretion of the treating physician to ensure patient safety and appropriate blood pressure control.

The primary objective of the EMBRACE study is to assess the effect of renal denervation on clinically meaningful cardiovascular outcomes in this high-risk population. The primary endpoint is a hierarchical composite endpoint analyzed using a win-ratio methodology, comparing patients randomized to renal denervation versus standard care. This hierarchical clinical outcome framework allows prioritization of more severe and clinically relevant events over less severe outcomes, providing an integrated assessment of net clinical benefit. The hierarchical outcome includes major adverse cardiovascular and cerebrovascular events such as death and other serious cardiovascular outcomes, followed by additional clinically relevant events as defined in the study protocol.

Secondary objectives of the EMBRACE study include evaluation of blood pressure control, changes in antihypertensive medication burden, renal safety, and procedure-related safety outcomes. Blood pressure measurements are obtained using standardized office blood pressure assessment methods at baseline and predefined follow-up intervals. Changes in blood pressure and medication use are evaluated as secondary and supportive endpoints, providing mechanistic context for observed clinical effects.

Safety endpoints include assessment of renal artery-related complications, access-site complications, renal function changes, and other adverse events related to renal denervation and percutaneous coronary intervention. Clinical events are collected throughout the follow-up period to allow comprehensive evaluation of both efficacy and safety.

The EMBRACE study is conducted in accordance with the principles of the Declaration of Helsinki, Good Clinical Practice guidelines, and applicable regulatory requirements. Written informed consent is obtained from all participants prior to performance of any study specific procedures. Study oversight is provided through standardized monitoring and safety reporting mechanisms to ensure data integrity and participant safety.

By integrating renal denervation into the staged PCI care pathway, EMBRACE seeks to address an important unmet clinical need in patients with advanced coronary artery disease and uncontrolled hypertension. The study aims to provide clinical evidence regarding the safety and effectiveness of renal denervation in this population and to clarify the potential role of this intervention as an adjunct to contemporary revascularization and pharmacologic treatment strategies.

The results of EMBRACE may inform future treatment approaches for patients with multivessel coronary artery disease and persistent hypertension, a population at particularly high risk for adverse cardiovascular outcomes. If renal denervation demonstrates meaningful and durable blood pressure reduction without compromising procedural safety, it may represent an important therapeutic option to optimize cardiovascular risk reduction in these patients.

List of abbreviation:

PCI - Percutaneous Coronary Intervention SoC - Standard of Care MACCE - Major Adverse Cardiovascular and Cerebrovascular Events MACE - Major Adverse Cardiovascular Events

02

Conditions studied

  • Multivessel Coronary Artery Disease
  • Hypertension Resistant to Conventional Therapy
03

In context

Hypertension Resistant to Conventional Therapy

47 studies on the registry are indexed under Hypertension Resistant to Conventional Therapy; 3 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 57 across 36 interventional studies indexed under Hypertension Resistant to Conventional Therapy.

Browse Hypertension Resistant to Conventional Therapy studies →

Lead sponsor

Ceric Sàrl is the lead sponsor of 17 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
21 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

  • Subject with multi-vessel disease
  • Having successful index PCI and planned staged procedure within 1-6 weeks to complete revascularization
  • Subjects ≥21 years of age
  • Office systolic blood pressure at index procedure and/or staged procedure (systolic blood pressure >140 mmHg) while taking 2 or more antihypertensive drugs
  • Subject agrees to have all study procedures performed, and is competent and willing to provide written, to participate in this clinical study prior to staged procedure

Exclusion criteria

Exclusion Criteria:

  • - for RDN outlined by IFU
  • Acute MI at time of the staged PCI procedure (AMI at time of the index PCI is allowed)
  • Subject has undergone prior renal denervation.
  • Subject has renal artery anatomy that is ineligible for RDN treatment per Symplicity Spyral™ IFU
  • Known secondary cause (e.g., renal artery stenosis, primary aldosteronism, pheochromocytoma, Cushing's syndrome, or other identifiable etiologies).
  • Severe renal failure ( \<30 ml/min/1.73 m²)
  • Known \<30%
  • Known history of polycystic kidney disease, unilateral kidney, or undergone renal transplant
  • Mechanical circulatory support during PCI
  • Subject is under judicial protection, tutorship or curatorship
  • Failure of index procedure
  • Acute MI, severe renal failure, need for mechanical circulatory support, or legal incapacity between the index and staged procedures resulting in loss of eligibility.
Terms in these criteria, in plain language(4)

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.

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.

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.

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.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
1,000 participants (estimated)

Study arms

  • Experimental
    Renal denervation

    Renal denervation (patient continue hypertension medication if applicable)

    Device: Renal denervation

  • No intervention
    Control

    Standard of care (patient continue hypertension medication if applicable)

Interventions

  • DeviceRenal denervation

    Catheter-based renal denervation performed during a standard renal artery catheterization procedure using a dedicated renal denervation system, according to the study protocol. The procedure is performed in addition to ongoing antihypertensive medical therapy, which is continued throughout the study as clinically indicated.

06

What researchers measure

Primary outcomes

  1. Primary endpoint: Win Ratio of Hierarchical Composite Endpoint After Staged PCI

    The primary endpoint will be assessed using a win ratio, a statistical method that compares treatment groups based on a hierarchical evaluation of clinically ordered outcomes. Patients will be compared pairwise between treatment groups, and outcomes will be evaluated in the following predefined order of clinical importance after staged PCI: Cardiovascular death Stroke Myocardial infarction Number of hospitalizations for heart failure Hospitalization for hypertensive crisis (yes/no) Number of hypertensive emergencies Change in office systolic blood pressure Change in antihypertensive medication (increase, no change, or decrease in number and/or dosage) For each patient pair, the first outcome in the hierarchy that differs between patients will determine the winner. The win ratio will be calculated as the total number of wins in the investigational treatment group divided by the total number of wins in the control group.

    Time frame: 2 Years post procedure

  2. Primary safety endpoint : Major vascular access site complications

    Number of participants who experience Major vascular access site complications within 30 d after the staged PCI.

    Time frame: 30 days after staged PCI

  3. Primary safety endpoint: Contrast-associated acute kidney injury (CA-AKI) (≥25% increase in serum creatinine within 48-72 hours)

    Number of patient having ≥25% increase in serum creatinine within 48-72 hours after the procedure

    Time frame: 30 days after staged PCI

  4. Primary safety endpoint: Renal artery complications

    Number of patients with renal artery complications (dissection requiring intervention) and renal artery stenosis (requiring intervention)

    Time frame: 30 days after staged PCI

Secondary outcomes

  1. Secondary endpoint

    \- ambulatory blood pressure change (increase - no change or decrease) between groups

    Time frame: 2, 3 & 5 Years after procedure

  2. Secondary endpoints: Quality of life

    improvement of QoL (EQ-5D-5L)

    Time frame: 2, 3 & 5 years after staged PCI

  3. Secondary endpoints: Health economics

    Incremental Cost-Effectiveness Ratio (enal denervation plus standard of care versus standard of care alone)

    Time frame: 2, 3 & 5 years after staged PCI

  4. Secondary endpoint: Time to first hypertension emergency

    A hypertensive crisis is defined by 2018 ESC/ESH Guidelines as a unplanned hospitalization due to severe elevation in blood pressure, typically ≥ 180 mmHg systolic and/or ≥ 120 mmHg diastolic, encompassing both hypertensive emergencies and hypertensive urgencies.

    Time frame: 2, 3 & 5 Years

  5. Secondary endpoint: kidney function

    eGFR measurement

    Time frame: 2, 3, 5 Years

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07602790
Lead sponsor
Ceric Sàrl
Responsible party
Sponsor
First posted
May 22, 2026
Start date
Nov 2026 (estimated)
Primary completion
Nov 2030 (estimated)
Completion
Nov 2033 (estimated)
Last update
May 22, 2026

Study contacts

Estelle Darrau, Ph.D
Contact
edarrau@cerc-europe.org
0675657408 ext. +33
laure Morsiani, Ph.D
Contact
lmorsiani@cerc-europe.org
0176739236 ext. +33
Felix Mahfoud, Prof.
principal investigator · Departement Biomedizin DBM Hebelstrasse
Roxana Mehran, Prof.
principal investigator · Icahn School of Medicine at Mount Sinai

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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