πŸ›οΈ Verified NIH Record β€’ Updated 2025-07-15

Long Term Follow Up for CTSN Mitral Valve Repair Studies (NCT03066050)

Long-Term Follow-Up For Participants Of: Evaluation Of Outcomes Following Mitral Valve Repair/Replacement In SMR and Surgical Interventions For MMR Trials

πŸ”΅ Active, Not Recruiting Interventional Protocol πŸ“Š Observational Clinical Research Sponsor: Icahn School of Medicine at Mount Sinai

🩺 Plain-English Summary (8th-Grade Level)

This study is a continuation of two previous studies --- the Severe Ischemic Mitral Regurgitation (SMR) Trial (NCT00807040) and the Moderate Ischemic Mitral regurgitation (MMR) Trial (NCT00806988) --- to learn more about patients' health 5-10 years after their mitral valve surgeries. The investigators will collect long-term health information on SMR and MMR trial participants using electronic medical records, patient and/or family input, public records, and healthcare- and vital status-related databases.

Who can join: Review the eligibility criteria below.

Location: University of Southern California β€” Los Angeles, California

Age range: 18 Years

πŸ§ͺ Interventions in This Study

  • MV Repair (OTHER)
  • MV Replacement (OTHER)
  • CABG (OTHER)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (24 Sites)

  • University of Southern California β€” Los Angeles, California
  • Emory University β€” Atlanta, Georgia
  • University of Maryland β€” Baltimore, Maryland
  • Suburban Hospital β€” Bethesda, Maryland
  • Brigham and Women's Hospital β€” Boston, Massachusetts
  • Columbia University Medical Center β€” New York, New York
  • Montefiore Einstein Heart Center β€” The Bronx, New York
  • Mission Hospital β€” Asheville, North Carolina
  • Duke University β€” Durham, North Carolina
  • East Carolina Heart Institute β€” Greenville, North Carolina
  • Cleveland Clinic Foundation β€” Cleveland, Ohio
  • Ohio State University β€” Columbus, Ohio
  • University of Pennsylvania β€” Philadelphia, Pennsylvania
  • Baylor Research Institute β€” Plano, Texas
  • University of Virginia Health Systems β€” Charlottesville, Virginia
  • Inova Heart and Vascular Institute β€” Falls Church, Virginia
  • University of Alberta Hospital β€” Edmonton, Alberta
  • Sunnybrook Health Science Centre β€” Toronto, Ontario
  • Saint Michael's Hospital β€” Toronto, Ontario
  • Toronto General Hospital β€” Toronto, Ontario
  • Montreal Heart Institute β€” Montreal, Quebec
  • Centre Hospitalier de l'UniversitΓ© de MontrΓ©al β€” Montreal, Quebec
  • HΓ΄pital du SacrΓ©-CΕ“ur de MontrΓ©al β€” Montreal, Quebec
  • Institut Universitaire de Cardiologie de Quebec (Hopital Laval) β€” QuΓ©bec,

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—