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Efficacy of Self-expandable and Balloon-expandable Valves in Patients With Ascending Aortic Dilation

Key facts

Where
Beijing, Kunming, and Shenzhen, ChinaSee the 3 sites

Where in China

  • National Center for Cardiovascular Disease, China & Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical CollegeBeijing, ChinaContact: Kang An, MDTaking people
  • Fuwai Yunnan Cardiovascular HospitalKunming, ChinaContact: Wenbin Ouyang, MDNot yet recruiting
  • Fuwai Shenzhen HospitalShenzhen, ChinaContact: Shiguo Li, MDNot yet recruiting

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
China National Center for Cardiovascular Diseases
Trial code
NCT06743568
Record updated
20 December 2024
Original description
This study evaluated the efficacy of self-expandable valves and balloon-expandable valves in patients with ascending aortic dilation who undergo transcatheter aortic valve replacement.Read full original descriptionShow less

This study evaluated the efficacy of self-expandable valves and balloon-expandable valves in patients with ascending aortic dilation who undergo transcatheter aortic valve replacement.

Inclusion: Severe AS defined as an aortic valve area (AVA) of 1cm2 or less or an indexed AVA of 0.6 cm2/m2 or less; Evaluation and selection for TAVR by the multidisciplinary heart team; Maximum ascending aortic diameter between 45mm and 54mm on preoperative contrast-enhanced computed tomography (CT) scan; Anatomic suitability for a transfemoral vascular access; Life expectancy of more than 12 months; Age ≥65 years.

Exclusion: Emergent surgery; History of surgical or transcatheter aortic valve replacement (valve in valve); History of any aortic surgery; Pure aortic regurgitation; Patients who refused to be randomized or unable to complete regular follow-up.

ClinicalTrials.gov NCT06743568