Registry evaluating long-term outcomes of Transcatheter aortic valve replacement

a Multinational Multicenter Prospective Transpacific TAVR Registry

Observational Asan Medical Center · NCT03826264

This study looks at how well Transcatheter Aortic Valve Replacement (TAVR) works for patients over time in real-life situations.

Quick facts

Study typeObservational
Enrollment10000 (estimated)
Ages19 Years and up
SexAll
SponsorAsan Medical Center Academic / other
Locations7 sites (Stanford, California and 6 other locations)
Trial IDNCT03826264 on ClinicalTrials.gov

What this trial studies

This registry assesses the long-term outcomes of patients undergoing Transcatheter Aortic Valve Replacement (TAVR) in real-world clinical settings. It is connected to the Asian TAVR registry, allowing for a comprehensive follow-up of subjects over a decade. The study aims to gather data that reflects the effectiveness and safety of TAVR procedures outside of controlled clinical trials.

Who should consider this trial

Good fit: Ideal candidates for this registry are all patients who are undergoing TAVR and can provide informed consent.

Not a fit: Patients who are not undergoing TAVR or cannot provide informed consent may not benefit from this registry.

Why it matters

Potential benefit: If successful, this registry could provide valuable insights into the long-term effectiveness and safety of TAVR, potentially improving patient outcomes.

How similar studies have performed: Other studies have shown success with similar observational approaches, particularly in evaluating long-term outcomes of TAVR.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* All patients undergoing TAVR
* Informed consent

Where this trial is running

Stanford, California and 6 other locations

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Heart Valve DiseasesAortic Valve InsufficiencyTAVRTAVIreal-world
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.