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Recruiting

NCT Number: NCT01390675

Anesthesia for Catheter Aortic Valve ImplantATIOn Registry

In modern cardiac surgery and cardiology Transcatheter Aortic Valve Implantation (TAVI) is an emerging procedure for high-risk patients that are assumed to be otherwise inoperable. The investigators want to evaluate the specific intraoperative anesthesiologic characteristics cardiac anesthesiologists have to face during these procedures.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Deutsches Herzzentrum München, Department of Anaesthesiology, Technische Universität München

Munich, Bavaria, D-80636, Germany

Location status: Recruiting

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients undergoing transcatheter aortic valve implantation (TAVI)

Exclusion criteria

  • Refusal by patient

Treatment and study plan

Primary outcomes

  1. Perioperative Care

    Time frame: 1 day

    major critical adverse events

Secondary outcomes

  1. Up to 10 years

    Time frame: 10 Years

    all-cause mortality

Study contacts

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

Michael Joner, M.D.,Prof

CONTACT

[email protected]

+49 89 1218

Patrick N Mayr, M.D.

CONTACT

[email protected]

+49 89 1218

Sponsors and collaborators

Lead sponsor

Deutsches Herzzentrum Muenchen

Other

Registry information

Acronym: AVIATOR

Important dates

Study start
2011
Primary completion
2026
Study completion
2027
First posted
Jul 11, 2011
Registry last updated
Aug 7, 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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