Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Long Term Follow Up for CTSN Mitral Valve Repair Studies
NCT03066050 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- OTHER MV Repair
- OTHER MV Replacement
- OTHER CABG
Study Locations (20)
North Carolina
- Mission Hospital — Asheville
- Duke University — Durham
- East Carolina Heart Institute — Greenville
Ontario
- Sunnybrook Health Science Centre — Toronto
- Saint Michael's Hospital — Toronto
- Toronto General Hospital — Toronto
Maryland
- University of Maryland — Baltimore
- Suburban Hospital — Bethesda
New York
- Columbia University Medical Center — New York
- Montefiore Einstein Heart Center — The Bronx
Ohio
- Cleveland Clinic Foundation — Cleveland
- Ohio State University — Columbus
Virginia
- University of Virginia Health Systems — Charlottesville
- Inova Heart and Vascular Institute — Falls Church
California
- University of Southern California — Los Angeles
Georgia
- Emory University — Atlanta
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 368 participants |
| Start Date | 2017-05-03 |
| Est. Completion | 2027-07-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03066050
The ClinicalTrials.gov registry entry for NCT03066050 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, 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 368 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Icahn School of Medicine at Mount Sinai, which has 946 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Coronary Artery Disease appearing as the primary indexed condition, and to 3 interventions — of which MV Repair 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: NCT03066050 reports 20 study locations spanning 12 distinct geographic areas — top geographies include North Carolina, Ontario, Maryland. 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 NCT03066050 about?
NCT03066050 is a clinical study titled "Long Term Follow Up for CTSN Mitral Valve Repair Studies". 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 investigato...
What is the current status of trial NCT03066050?
This trial is currently active not recruiting. The enrollment target is 368 participants. The study started on 2017-05-03. Estimated completion is 2027-07-31.
What conditions does trial NCT03066050 study?
This clinical trial studies the following conditions: Coronary Artery Disease, Mitral Valve Insufficiency. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03066050?
The interventions under investigation include: MV Repair (OTHER), MV Replacement (OTHER), CABG (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03066050?
This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 946 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03066050 being conducted?
This trial has 20 study locations across California, Georgia, Maryland, Massachusetts, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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