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REvascularization CHoices Among Under-Represented Groups Evaluation: The RECHARGE Trial - Women
NCT06399692 · View on ClinicalTrials.gov ↗
Study Summary
This is a research study in women 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.
Conditions Studied
Interventions
- PROCEDURE Coronary artery bypass grafting (CABG)
- PROCEDURE Percutaneous coronary intervention (PCI)
Study Locations (18)
New York
- NewYork-Presbyterian Hospital - Queens — Flushing
- Icahn School of Medicine - Mount Sinai Morningside — New York
- Icahn School of Medicine - Mount Sinai Hospital — New York
- Columbia University Irving Medical Center/NewYork-Presbyterian Hospital — New York
- Weill Cornell Medicine / NYPH — New York
- Westchester Medical Center — Valhalla
Kentucky
- Baptist Health Lexington — Lexington
- Baptist Health Louisville — Louisville
Tennessee
- Methodist Le Bonheur Healthcare — Memphis
- Ascension Saint Thomas Hospital — Nashville
California
- Adventist Health Glendale — Glendale
Georgia
- Emory University — Atlanta
Indiana
- Ascension St. Vincent Cardiovascular Research Institute — Carmel
Massachusetts
- Massachusetts General Hospital — Boston
New Jersey
- Englewood Hospital — Englewood
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 600 participants |
| Start Date | 2024-09-16 |
| Est. Completion | 2039-01-01 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06399692
The ClinicalTrials.gov registry entry for NCT06399692 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 679 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Coronary Artery Disease appearing as the primary indexed condition, and to 2 interventions — of which Coronary artery bypass grafting (CABG) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06399692 reports 18 study locations spanning 11 distinct geographic areas — top geographies include New York, Kentucky, Tennessee. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06399692 about?
NCT06399692 is a clinical study titled "REvascularization CHoices Among Under-Represented Groups Evaluation: The RECHARGE Trial - Women". This is a research study in women 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 op...
What is the current status of trial NCT06399692?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 600 participants. The study started on 2024-09-16. Estimated completion is 2039-01-01.
What conditions does trial NCT06399692 study?
This clinical trial studies the following conditions: Coronary Artery Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06399692?
The interventions under investigation include: Coronary artery bypass grafting (CABG) (PROCEDURE), Percutaneous coronary intervention (PCI) (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06399692?
This trial is sponsored by Weill Medical College of Cornell University, which has 679 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06399692 being conducted?
This trial has 18 study locations across California, Georgia, Indiana, Kentucky, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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