Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Glendale, California and other locations
Dates
study started
study ends around

Description

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.

Details

The RECHARGE: Women Trial is a multicenter, 1:1 randomized, open-label superiority trial.

Patients meeting the eligibility criteria for whom there is equipoise for revascularization with CABG and PCI, as determined by the local Heart Team, will be included. Participants will be followed for 5-10 years. Telephone follow-up will be conducted by the a central follow-up coordinating center at 30 days, 3 months, 6 months, and thereafter every 6 months through 36 months post-randomization. After 36 months, follow-up will be performed every year (48, 60, 72, 84, 96, 108, 120 months). A repeat transthoracic echocardiogram and blood draw for serum creatinine, hemoglobin and lipids should be performed at 1 year, as per standard of care, at either an out-patient facility or in a hospital.

Keywords

Coronary Artery Disease, RECHARGE, Cardiac Surgery, coronary artery bypass grafting, percutaneous coronary intervention, Quality of Life, Coronary Artery Bypass, Coronary artery bypass grafting (CABG), Percutaneous coronary intervention (PCI), RECHARGE:Women - CABG, RECHARGE:Women - PCI

Eligibility

You can join if…

Open to people ages 18 years and up

  1. Female sex
  2. Patient is at least 18 years old.
  3. 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.
  4. Ability to provide written informed consent and comply with all follow-up procedures, including QOL questionnaires.

You CAN'T join if...

  1. ST-segment elevation MI within 3 days
  2. Cardiogenic shock
  3. Prior PCI within 1 year or any prior CABG anytime
  4. Planned hybrid revascularization (PCI after CABG or CABG after PCI)
  5. Planned single vessel revascularization (other than isolated left main disease)
  6. Need for any cardiac surgical or interventional procedure other than coronary revascularization at the present time or anticipated within 3 years
  7. 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
  8. 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
  9. Current participation in another investigational drug or device study that has not reached its primary endpoint
  10. Life-expectancy less than 3 years due to concomitant non-cardiac conditions
  11. 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.)

Locations

  • Adventist Health Glendale accepting new patients
    Glendale California 91206 United States
  • Baylor Scott and White accepting new patients
    Dallas Texas 75246 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Weill Medical College of Cornell University
Links
Sign up for this study
ID
NCT06399692
Phase
Phase 3 research study
Study Type
Interventional
Participants
Expecting 600 study participants
Last Updated