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NCT Number: NCT06743568

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

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.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

National Center for Cardiovascular Disease, China & Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, Beijing Municipality, China

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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 criteria

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

Treatment and study plan

Transcatheter Aortic Valve Replacement

Device

Eligible patients will be randomized 1:1 to self-expandable valve group or balloon-expandable valve group.

Primary outcomes

  1. Device success

    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).

  2. 30-day all-cause mortality

    Time frame: 30 days

    30-day all-cause mortality

  3. 30-day adverse aortic events

    Time frame: 30 days

    Aortic-related death, aortic dissection, or aortic rupture.

Secondary outcomes

  1. 1-year all-cause mortality

    Time frame: 1 year

    1-year all-cause mortality

  2. 1-year cardiovascular mortality

    Time frame: 1 year

    1-year cardiovascular mortality

  3. 1-year adverse aortic events

    Time frame: 1 year

    Aortic-related death, aortic dissection, or aortic rupture.

  4. Aortic expansion rate≥3mm/year

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Kang An, MD

CONTACT

[email protected]

+86-15801301740

Sponsors and collaborators

Lead sponsor

China National Center for Cardiovascular Diseases

Other Gov

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Dec 20, 2024
Registry last updated
Dec 20, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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