Actively Recruiting
Transcatheter Aortic Valve Replacement Single Center Registry in Chinese Population
Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2021-07-15
2000
Participants Needed
1
Research Sites
578 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to evaluate the safety and effectiveness of transcatheter aortic valve replacement in Chinese population.
CONDITIONS
Official Title
Transcatheter Aortic Valve Replacement Single Center Registry in Chinese Population
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with symptomatic aortic stenosis or regurgitation
- Subject has been informed of the nature of the study, agrees to its provisions and has provided written informed consent
- The subject agrees to comply with specified follow-up evaluations and to return to the investigational site where the procedure was performed
- Patients are technically and anatomically eligible for interventions
You will not qualify if you...
- Known hypersensitivity or contraindication to aspirin, heparin (HIT/HITTS), bivalirudin, nitinol (titanium or nickel), ticlopidine, clopidogrel, or contrast media that cannot be adequately pre-medicated
- Subject refuses a blood transfusion
- Other medical, social, or psychological conditions that preclude appropriate consent according to the Investigator
- Life expectancy is less than one year
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The Second Affiliated Hospital, School of Medicine at Zhejiang University
Hanzhou, Zhejiang, China, 310000
Actively Recruiting
Research Team
X
Xianbao Liu, MD
CONTACT
J
Jian-an Wang, MD,PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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