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Active, not recruiting No phase listed Observational

Long Term Follow Up for CTSN Mitral Valve Repair Studies

ClinicalTrials.gov ID: NCT03066050

Public ClinicalTrials.gov record NCT03066050. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 13, 2026, 1:07 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT03066050
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Enrollment
368 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 2, 2017
Primary completion
Jul 30, 2027
Completion
Jul 30, 2027
Last update posted
Jul 15, 2025

2017 – 2027

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
University of Southern California Los Angeles California 90033
Emory University Atlanta Georgia 30308
University of Maryland Baltimore Maryland 21201
Suburban Hospital Bethesda Maryland 20814
Brigham and Women's Hospital Boston Massachusetts 02115
Columbia University Medical Center New York New York 10032
Montefiore Einstein Heart Center The Bronx New York 10467
Mission Hospital Asheville North Carolina 28801
Duke University Durham North Carolina 27710
East Carolina Heart Institute Greenville North Carolina 27834
Cleveland Clinic Foundation Cleveland Ohio 44195
Ohio State University Columbus Ohio 43210
University of Pennsylvania Philadelphia Pennsylvania 19104
Baylor Research Institute Plano Texas 75093
University of Virginia Health Systems Charlottesville Virginia 22908
Inova Heart and Vascular Institute Falls Church Virginia 22042

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03066050, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 15, 2025 · Synced Sep 13, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03066050 live on ClinicalTrials.gov.

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