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Multi Center Registry of Transcatheter Aortic Valve Replacement in Northeast China

Severe Aortic Valve Stenosis Clinical Trial

Official title:
Multi Center Registry of Transcatheter Aortic Valve Replacement in Northeast China

Clinical Trial Summary

The purpose of this study was to observe the safety and effectiveness of transcatheter aortic valve replacement in patients with aortic valve stenosis in a real-world clinical practice environment.

Clinical Trial Description

This study is a prospective / retrospective, multicenterstudy after listing. The researchers preliminarily confirmed that they could be enrolled in this study according to the diagnosis of the subjects' medical history. After fully informed, they signed the informed consent, and met the TAVR inclusion requirements (see the inclusion criteria for details). At the same time, they registered the subjects in multiple centers. After the start of the trial, the participants were enrolled in the study, All the subjects who met the inclusion criteria but did not meet the discharge criteria were registered in the central registration system. The patients were followed up for 30 days, 6 months and 12 months, and followed up by telephone for 2, 3, 4 and 5 years. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04988243
Study type Interventional
Source CCRF Inc., Beijing, China
Contact
Status Not yet recruiting
Phase N/A
Start date August 2021
Completion date August 2028
View Details
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