Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04954404

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

Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2021-07-08

2000

Participants Needed

1

Research Sites

521 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with mitral valve disease confirmed by transthoracic echocardiogram and judged likely to benefit from intervention
  • Provided written informed consent after being informed about the study
  • Agree to comply with follow-up evaluations and return to the investigational site
  • Technical and anatomical eligibility for transcatheter mitral valve interventions
Not Eligible

You will not qualify if you...

  • Anatomically ineligible for intervention as judged by the investigator
  • Known allergy or contraindication to procedural medications that cannot be medically managed
  • Active endocarditis or active rheumatic heart disease
  • History of severe bleeding disorders or refusal of blood transfusions
  • Conditions preventing therapeutic benefit or life expectancy less than one year
  • Any disorder that affects ability to give informed consent or comply with study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Second Affiliated Hospital Zhejiang University School of Medicine.

Hangzhou, Zhejiang, China, 310006

Actively Recruiting

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Research Team

J

Jian'an Wang, PhD, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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