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NCT06399705RecruitingPhase 3

REvascularization CHoices Among Under-Represented Groups Evaluation: The RECHARGE Trial - Minorities

Source: ClinicalTrials.gov · Last updated 8 Sept 2026

Brief summary (registry, in English)

This is a research study in minorities to compare the outcomes of two procedures that restore blood flow to the arteries of the heart. In one procedure the blockages are ballooned and then stented with a small wire mesh tube through a small incision in the wrist or the groin. The other procedure is an open-heart operation in which healthy blood vessels from inside the chest, leg, and/or forearm are used to "bypass" the blockages (like a detour). Outcomes will be measured by comparing survival and improvement in quality-of-life.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
600 (estimated)
First submitted
30 Apr 2024
Start date
Oct 2024
Primary completion date
Mar 2033
Lead sponsor
Weill Medical College of Cornell University
NCT number
NCT06399705

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 600
  • From Oct 2024 to the primary completion date, Mar 2033
  • 18 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior PCI within 1 year or any prior CABG anytime
  • Pregnancy (women of child-bearing potential must have a negative pregnancy test within 1 week before randomization) or intent to become pregnant within 1 year after randomization
  • Current participation in another investigational drug or device study that has not reached its primary endpoint
  • Life-expectancy less than 3 years due to concomitant non-cardiac conditions

Other illness

  • Planned single vessel revascularization (other than isolated left main disease)
  • Need for any cardiac surgical or interventional procedure other than coronary revascularization at the present time or anticipated within 3 years, with the exception that surgical or interventional left atrial appendage ligation or occlusion and/or atrial fibrillation ablation may be performed at site discretion either during or subsequent to the index revascularization procedure
  • Unable to tolerate, obtain or comply with dual antiplatelet therapy for at least 3 months if presentation with stable CAD or 6 months if presentation with a troponin-positive acute coronary syndrome
  • Any condition(s) are present that are likely to interfere with the study protocol procedures including medication adherence and follow-up through 10 years (e.g. mental disability, substance abuse, anticipated international relocation, etc.)

Other

  • ST-segment elevation MI within 3 days
  • Cardiogenic shock
  • Planned hybrid revascularization (PCI after CABG or CABG after PCI)

Who the study is looking for

  • Patient must identify as Black race or Hispanic ethnicity
  • Patient is at least 18 years old.
  • Multivessel or left main CAD is present for which revascularization is intended and for which there is equipoise between CABG and PCI according to local Heart Team assessment.
  • Ability to provide written informed consent and comply with all follow-up procedures, including QOL questionnaires.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (18)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emory University
Coordinator of this site? Confirm its status
AtlantaUnited StatesRecruiting
Massachusetts General Hospital
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BostonUnited StatesRecruiting
Ascension St. Vincent Cardiovascular Research Institute
Coordinator of this site? Confirm its status
CarmelUnited StatesRecruiting
Ohio State University
Coordinator of this site? Confirm its status
ColumbusUnited StatesRecruiting
Baylor Scott and White
Coordinator of this site? Confirm its status
DallasUnited StatesRecruiting
Duke University
Coordinator of this site? Confirm its status
DurhamUnited StatesRecruiting
Englewood Hospital
Coordinator of this site? Confirm its status
EnglewoodUnited StatesRecruiting
NewYork-Presbyterian Hospital - Queens
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FlushingUnited StatesRecruiting
Adventist Health Glendale
Coordinator of this site? Confirm its status
GlendaleUnited StatesRecruiting
Baptist Health Lexington
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LexingtonUnited StatesRecruiting
Baptist Health Louisville
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LouisvilleUnited StatesRecruiting
Methodist Le Bonheur Healthcare
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MemphisUnited StatesRecruiting
Ascension Saint Thomas Hospital
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NashvilleUnited StatesRecruiting
Icahn School of Medicine - Mount Sinai Hospital
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Columbia University Irving Medical Center / NewYork-Presbyterian Hospital
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Icahn School of Medicine - Mount Sinai Morningside
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Weill Cornell Medicine/NewYork-Presbyterian Hospital
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Westchester Medical Center
Coordinator of this site? Confirm its status
ValhallaUnited StatesRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.