Mitral Regurgitation Clinical Trials
16 studies are recruiting for mitral regurgitation in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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Cephea Early Feasibility Study
The objective of this study is to evaluate the preliminary safety and effectiveness of the Cephea Mitral Valve System for the treatment of symptomatic patients with mitral valve disease (including mitral regurgitation, mitral stenosis and mixed mitral valve disease) in whom transcatheter therapy is…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Banner-University Medical Center Phoenix, Phoenix, Arizona
- Locations
- 22 in total
- Run by
- Abbott Medical Devices
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Abbott Cephea Mitral Valve Disease Registry
The objective of this registry is to gather clinical data on symptomatic patients with mitral valve disease, including patients with mitral regurgitation, mitral stenosis, and mixed mitral valve disease. Data collected from this registry are expected to improve our understanding of the impact of co…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University Hospital - Univ. of Alabama at Birmingham (UAB), Birmingham, Alabama
- Locations
- 24 in total
- Run by
- Abbott Medical Devices
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EFS of Posterior Leaflet Replacement to Reduce Mitral Regurgitation (United States)
The goal of this early feasibility clinical trial is to learn if the device MR-ace Implant and Delivery System works in patients with moderate or severe mitral valve regurgitation. It will also learn about the safety of the device MR-ace Implant and Delivery System. The main questions it aims to an…
- Stage
- Not phased
- Ages
- 21 and older
- Site
- Emory Midtown, Atlanta, Georgia
- Locations
- 3 in total
- Run by
- Polares Medical SA
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Reduction or Elimination of Mitral Regurgitation With the SATURN TMVR System (CASSINI-US)
CASSINI-US is a prospective, single-arm, multicenter early feasibility study enrolling up to 15 patients at up to 5 sites in the United States (US). The purpose of the study is to evaluate the technical (implant) feasibility, and safety, and performance of the SATURN TS TMVR System for the treatmen…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Los Robles Regional Medical Center, Thousand Oaks, California
- Locations
- 5 in total
- Run by
- InnovHeart
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ATLAS (AltaValve) Pivotal Trial
This is a prospective, single arm, multicenter, clinical trial designed to evaluate the safety and performance of the AltaValve System for the treatment of mitral regurgitation in a targeted patient population.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Banner University Medical Center, Phoenix, Arizona
- Locations
- 58 in total
- Run by
- 4C Medical Technologies, Inc.
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The CardioClip Study
The CardioClip study is exploring the use of a wireless sensor to monitor pressure in the pulmonary artery. This sensor is inserted much like the mTEER procedure, a non-surgical method through a vein in the groin. The investigators want to find out if the sensor, by constantly sending information a…
- Stage
- Not phased
- Ages
- 18 to 90
- Site
- Columbia University Irving Medical Center / NewYork-Presbyterian Hospital, New York, New York
- Run by
- Columbia University
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Annuloplasty Rings and Band Post-Market Clinical Follow-Up Study
ARB-PMCF is a multicenter, observational study of the safety and performance of Abbott annuloplasty devices used in surgical repair of mitral and tricuspid valve regurgitation. The devices included in this study are the SJM™ Rigid Saddle Ring and SJM Séguin Annuloplasty Ring, indicated for mitral v…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Tartu University Hospital, Tartu,
- Locations
- 17 in total
- Run by
- Abbott Medical Devices
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CHoice of OptImal transCatheter trEatment for Mitral Insufficiency Registry
This multinational, investigator-initiated registry aims to investigate clinical outcomes of patients undergoing transcatheter mitral valve replacement (TMVR). The registry primarily focuses on patients treated with TMVR in real-world clinical practice. Patients evaluated for TMVR but not undergoin…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Tucson Medical Center, Tucson, Arizona
- Locations
- 43 in total
- Run by
- Universitätsklinikum Hamburg-Eppendorf
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Transcatheter Mitral Valve Repair for Inotrope Dependent Cardiogenic Shock
Mitral regurgitation may be seen in the setting of cardiogenic shock. Transcatheter edge-to-edge repair (TEER) has been shown to improve outcomes in patients with chronic heart failure. Observational studies suggest improvements in clinical outcomes in patients with mitral regurgitation in the sett…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Mayo Clinic, Rochester, Minnesota
- Locations
- 4 in total
- Run by
- Ottawa Heart Institute Research Corporation
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A Clinical Study of GeminiOne TEER System for the Treatment of Severe, Symptomatic MR.
To confirm the effectiveness and safety of the GeminiOne Transcatheter Mitral Valve Repair System for the treatment of severe, symptomatic mitral regurgitation.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Los Robles Regional Medical Centre, Thousand Oaks, California
- Run by
- Sierra Valve LLC
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The ENCIRCLE Trial
This study will establish the safety and effectiveness of the SAPIEN M3 System in subjects with symptomatic, at least 3+ mitral regurgitation (MR) for whom commercially available surgical or transcatheter treatment options are deemed unsuitable. Following completion of enrollment, subjects will be …
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Laval University, Québec, Quebec
- Locations
- 68 in total
- Run by
- Edwards Lifesciences
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EFS of the CardioMech MVRS
Safety and performance evaluation of the CardioMech Mitral Valve Repair System (MVRS) in patients with degenerative mitral valve regurgitation.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Northwestern University, Evanston, Illinois
- Locations
- 12 in total
- Run by
- CardioMech AS
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The MITRAL II Pivotal Trial (Mitral Implantation of TRAnscatheter vaLves).
A prospective multicenter study enrolling high surgical risk patients with severe mitral annular calcification (MAC) and symptomatic mitral valve dysfunction (severe stenosis, ≥ moderate to severe regurgitation, or mixed ≥ moderate stenosis and ≥ regurgitation). There are 2 Arms in this study: 1) "…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Dignity Health Chandler Regional Medical Center, Gilbert, Arizona
- Locations
- 17 in total
- Run by
- Mayra Guerrero
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Novel Characterization of Sex Specific Biologic Signatures in Valvular Heart Disease
This project aims to validate sex-specific biologic signatures associated with aortic valve disease developed in a large multicenter CMR registry, using unsupervised phenomapping. The aim to use standard and advanced CMR techniques (MRF, DTI, chemical exchange transfer, and radiomics analysis) is t…
- Stage
- Not phased
- Ages
- 18 to 90
- Site
- Cleveland Clinic, Cleveland, Ohio
- Run by
- The Cleveland Clinic
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Use of Phenylephrine for Assessment of Mitral Regurgitation Severity
The study proposes to develop a phenylephrine protocol to be used during transesophageal echocardiography, whereby intravenous phenylephrine would be used to increase afterload with the intent to mimic the awake hemodynamic profile and variation that occurs with normal physical activity. The expect…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Montefiore Medical Center, New York, New York
- Run by
- Montefiore Medical Center
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An Early Feasibility Study of the HighLife 28mm Trans-Septal Transcatheter Mitral Valve Replacement System
Study to evaluate the feasibility, safety and performance of the HighLife trans-septal Transcatheter Mitral Valve in patients with moderate-severe and severe mitral regurgitation who are at high risk for surgical treatment.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Tucson Medical Center, Tucson, Arizona
- Locations
- 10 in total
- Run by
- HighLife SAS
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.