Transcatheter Mitral Valve InterventiOn Single Center Registry in CHinese Patients With Mitral Valve Disease (TORCH-M)

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

The purpose of this study is to evaluate the safety and effectiveness of transcatheter mitral valve intervention in Chinese population with mitral valve disease.

Eligibility criteria

Qualifiers

Patients with mitral valve disease, as determined by the site from a transthoracic echocardiogram (TTE), and in the judgment of the investigator intervention is likely to provide clinical benefit for the patient.

Subject has been informed of the nature of the study, agrees to its provisions and has provided written informed consent.

The subject agrees to comply with specified follow-up evaluations and to return to the investigational site where the procedure was performed.

Patients are technical and anatomical eligible for interventions.

Disqualifiers

In the judgment of the investigator, subjects are not anatomical eligible for interventions.

Known hypersensitivity or contraindication to procedural medications which cannot be adequately managed medically.

Active endocarditis or active rheumatic heart disease.

History of severe bleeding diathesis or coagulopathy or subject will refuse blood transfusions.

Trial design

Treatments tested in this trial

  • transcatheter mitral valve repair/transcatheter mitral valve replacement

Treatment groups

2,000 Participants
are divided into 1 treatment group