Registry for anesthesia during transcatheter aortic valve implantation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational registry aims to evaluate the intraoperative anesthesiologic characteristics faced by cardiac anesthesiologists during transcatheter aortic valve implantation (TAVI) procedures. It focuses on high-risk patients who are typically considered inoperable and seeks to gather data on anesthesia management and outcomes. By documenting these experiences, the study aims to improve understanding and practices in anesthesia for TAVI. The study will include patients undergoing TAVI at a specialized cardiac center in Munich.

Why it matters

Who can join: the full rules

Inclusion Criteria:

\- Patients undergoing transcatheter aortic valve implantation (TAVI)

Exclusion Criteria:

\- Refusal by patient

Where it's running

• Deutsches Herzzentrum München, Department of Anaesthesiology, Technische Universität München
  Munich, Bavaria, Germany Recruiting

Study contacts

• Principal investigator: Patrick N Mayr, M.D. — Deutsches Herzzentrum München, Technische Universität München
• Study coordinator: Patrick N Mayr, M.D.
• Email: mayrp@dhm.mhn.de
• Phone: +49 89 1218

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.