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OpenTrials
Completed

NCT Number: NCT03104660

Coronary and Structural Interventions Ulm - Transcatheter Mitral Valve Repair (CSI-Ulm-TMVR)

To evaluate the long-term results after transcatheter mitral valve repair

Completed

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Key information

Conditions

Mitral Valve Regurgitation Cardiovascular Diseases Heart Diseases Heart Valve Diseases Mitral Valve Insufficiency

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Ulm

Ulm, 89081, Germany

About this study

Patients with transcatheter mitral valve repair are followed for 10 years to demonstrate efficacy and safety.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • mitral valve regurgitation
  • transcatheter mitral valve repair

Exclusion criteria

  • no written informed consent

Treatment and study plan

CE certified mitral valve repair systems

Device

Patients receive a transcatheter mitral valve repair with CE certified transcatheter mitral repair systems.

Primary outcomes

  1. Major adverse cerebral and cardiac events

    Time frame: 10 years

    Major adverse cerebral and cardiac events

Sponsors and collaborators

Lead sponsor

University of Ulm

Other

Registry information

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Apr 7, 2017
Registry last updated
Apr 28, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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