Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
ACTIVE NOT RECRUITING
NCT04982588
NA

Evolut PRO China Clinical Study

Sponsor: Medtronic Cardiovascular

View on ClinicalTrials.gov

Summary

Interventional study to evaluate the safety and efficacy of the Medtronic CoreValve™ Evolut™ PRO System when used by China implanting centers in Chinese patients with severe symptomatic aortic stenosis (AS) who are at high risk for Surgical Aortic Valve Replacement (SAVR).

Official title: Medtronic CoreValve™ Evolut™ PRO System China Clinical Study

Key Details

Gender

All

Age Range

65 Years - Any

Study Type

INTERVENTIONAL

Enrollment

52

Start Date

2021-07-17

Completion Date

2028-05-15

Last Updated

2025-12-03

Healthy Volunteers

No

Interventions

DEVICE

Medtronic CoreValve™ Evolut™ PRO System

The system comprised of the following three components: 1. CoreValve™ Evolut™ PRO Transcatheter Aortic Valve (TAV) 2. EnVeo™ PRO Delivery Catheter System (DCS) 3. EnVeo™ PRO Loading System (LS)

Locations (4)

Beijing Anzhen Hospital, Capital Medical University

Beijing, Beijing Municipality, China

Chinese PLA General Hospital, Chinese PLA Medical School

Beijing, Beijing Municipality, China

West China Hospital of Sichuan University

Chengdu, Sichuan, China

The Second Affiliated Hospital Zhejiang University School of Medicine

Hangzhou, Zhejiang, China