Transcatheter Aortic Valve Replacement Single Center Registry in Chinese Population
Recruiting now · Phase 4
Conditions studied: Symptomatic Aortic Stenosis
In brief
The purpose of this study is to evaluate the safety and effectiveness of transcatheter aortic valve replacement in Chinese population.
Key facts
- Study ID
- NCT02803294
- Run by
- Second Affiliated Hospital, Zhejiang University, School of Medicine
- People needed
- 2000
- Starts
- 2016-06-01
- Expected to finish
- 2027-07-01
- Last updated by the study team
- 2021-07-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with symptomatic aortic stenosis/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 technical and anatomical eligible for interventions
You may not qualify if…
- A known hypersensitivity or contraindication to any of the following which cannot be adequately pre-medicated: Aspirin Heparin (HIT/HITTS) and bivalirudin Nitinol (titanium or nickel) Ticlopidine and clopidogrel Contrast media
- Subject refuses a blood transfusion.
- Other medical, social, or psychological conditions that in the opinion of an Investigator precludes the subject from appropriate consent.
- Life expectancy is less than one year
Where it is running
- The Second Affiliated Hospital, School of Medicine at Zhejiang University — Hanzhou, Zhejiang, China (enrolling)
Full record on ClinicalTrials.gov
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