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Recruiting Observational

TAVR for Aortic Valve Disease

NCT05439863 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2022-07-01
Last updated
2024-11-15

Condition(s) studied

Aortic Valve Disease

Investigational drug(s) / intervention(s)

transcatheter heart valve

transcatheter heart valve: patients with severe aortic valve disease underwent transcatheter heart valve

Study summary

Transcatheter aortic valve replacement (TAVR) has became an important treatment of severe aortic stenosis (AS). Several randomized clinical trials showed that TAVR was non-inferior or superior to surgical aortic valve replacement (SAVR). However, many different issues have emerged: TAVR in younger patients? valve leaflet thrombosis? transcatheter valve durability? coronary reaccess after TAVR? TAVR in bicuspid aortic valve? TAVR in aortic regurgitation? etc. Hence, a prospective, multicenter database is created to provide the real-word data for these questions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Clinical diagnosis of severe aortic stenosis or aortic regurgitation 2. Patients undergo transcatheter aortic valve replacement Exclusion Criteria: patients refuse the clinical follow-up

Primary outcome measure(s)

  • all-cause death during follow-up — 5 years
    all-cause death during 5-year follow-up

Trial sites (1)

FacilityCityRegionStatus
Nanjing First Hospital Nanjing Jiangsu Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05439863 on ClinicalTrials.gov ↗ ← All trials in China