Prospective Multicenter Registry of Patients With Mitral Stenosis Undergoing Percutaneous Mitral Balloon Commissurotomy

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT07175532

Enrollment

400

Registered

2025-09-16

Start date

2025-05-01

Completion date

2031-12-31

Last updated

2025-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mitral Stenosis

Brief summary

The goal of this observational study is to learn about the clinical outcomes after percutaneous mitral balloon commissurotomy (PMBC) for patients with mitral stenosis (MS) using nation-wide multicenter prospective registry including tertiary-referral hospitals in Korea. The main question it aims to answer is: What is the clinical outcomes after PMBC? Which method is appropriate to determine inflated Inoue balloon size?

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 89 Years

Healthy volunteers

Inclusion criteria

* Patients with mitral stenosis undergoing PMBC

Exclusion criteria

* Patients who cannot understand this study due to mental illness * Serious comorbidity limiting life expectancy within 1 year * Limited activity (NYHA class III or IV) due to non-cardiac disease

Design outcomes

Primary

Measure	Time frame
Number of Participants with Treatment-Related Adverse Events	From enrollment to 1 year after PMBC

Countries

South Korea

Contacts

Primary ContactJong-Min Song

jmsong@amc.seoul.kr82230103168

Outcome results