Transcatheter Aortic Valve Replacement
DeviceEligible patients will be randomized 1:1 to self-expandable valve group or balloon-expandable valve group.
NCT Number: NCT06743568
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.
Interested in participating?
Request Info65 year and older
All sexes
Interventional
Not applicable
National Center for Cardiovascular Disease, China & Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, Beijing Municipality, China
Ascending aortic dilation (AAD) is a common feature in patients with aortic stenosis, especially in those with bicuspid aortic valve. According to the 2022 AHA/ACC Guideline for the Diagnosis and Management of Aortic Disease, in patients undergoing surgical aortic valve replacement who have a concomitant AAD with a maximum diameter of ≥45mm, ascending aortic replacement is reasonable when performed by experienced surgeons in a Multidisciplinary Aortic Team (Class 2a, Level B-NR). However, in patients undergoing transcatheter aortic valve replacement, the impact of ascending aortic dilation remains unclear. Therefore, we designed this multicenter prospective randomized controlled trial, aiming to assess the efficacy of self-expandable and balloon-expandable valves in patients with AAD with a maximum diameter of ≥45mm.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Eligible patients will be randomized 1:1 to self-expandable valve group or balloon-expandable valve group.
Time frame: Perioperative period
(1) freedom from mortality; (2) successful access, delivery of the device, and retrieval of the delivery system; (3) correct positioning of a single prosthetic heart valve into the proper anatomical location; (4) freedom from surgery or intervention related to the device or to a major vascular or access-related, or cardiac structural complication; (5) intended performance of the valve (mean gradient <20mmHg, peak velocity <3m/s, Doppler velocity index ≥0.25, and less than moderate aortic regurgitation).
Time frame: 30 days
30-day all-cause mortality
Time frame: 30 days
Aortic-related death, aortic dissection, or aortic rupture.
Time frame: 1 year
1-year all-cause mortality
Time frame: 1 year
1-year cardiovascular mortality
Time frame: 1 year
Aortic-related death, aortic dissection, or aortic rupture.
Time frame: 1 year
The aortic expansion rate was defined by the change of AA diameter (before the procedure and at the latest follow-up) divided by the follow-up period.
Contact information is provided by the study sponsor or research team.
China National Center for Cardiovascular Diseases
Other Gov
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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