Skip to content

TAVR for Aortic Valve Disease

Transcatheter Aortic Valve Replacement for Severe Aortic Valve Disease: Multi-center, Real-word Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05439863
Enrollment
5000
Registered
2022-06-30
Start date
2022-07-01
Completion date
2037-12-30
Last updated
2024-11-15

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

Conditions

Aortic Valve Disease

Brief 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.

Interventions

patients with severe aortic valve disease underwent transcatheter heart valve

Sponsors

Nanjing First Hospital, Nanjing Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
all-cause death during follow-up5 yearsall-cause death during 5-year follow-up

Secondary

MeasureTime frameDescription
cardiac death during follow-up5 yearsCardiac death during 5-year follow-up

Countries

China

Contacts

Primary ContactJun-Jie Zhang, MD
jameszll@163.com+86-25-52271350
Backup ContactJing Kan, MPH
kanjingok@126.com+86-25-52271398

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026