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Anesthesia for Catheter Aortic Valve ImplantATIOn Registry (AVIATOR)

This study is currently recruiting participants.
Verified August 2016 by N Patrick Mayr, Deutsches Herzzentrum Muenchen
Sponsor:
ClinicalTrials.gov Identifier:
NCT01390675
First Posted: July 11, 2011
Last Update Posted: July 26, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
N Patrick Mayr, Deutsches Herzzentrum Muenchen
  Purpose
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.

Condition
Heart Failure Excessive Amount of Blood / Fluid Transfusion Intraoperative Cardiac Arrest During Cardiac Surgery Critical Incident Anesthesia Failed Conscious Sedation During Procedure

Study Type: Observational
Study Design: Observational Model: Other
Time Perspective: Prospective

Further study details as provided by N Patrick Mayr, Deutsches Herzzentrum Muenchen:

Primary Outcome Measures:
  • Perioperative Care [ Time Frame: perioperative ]

Estimated Enrollment: 5000
Study Start Date: June 2011
Estimated Study Completion Date: December 2021
Estimated Primary Completion Date: December 2018 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients undergoing transcatheter aortic valve implantation (TAVI)
Criteria

Inclusion Criteria:

- Patients undergoing transcatheter aortic valve implantation (TAVI)

Exclusion Criteria:

- Refusal by patient

  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01390675


Contacts
Contact: Patrick N Mayr, M.D. +49 89 1218 ext 4611 mayrp@dhm.mhn.de
Contact: Peter Tassani, M.D., Ph.D +49 89 1218 ext 4611 tassani@dhm.mhn.de

Locations
Germany
Deutsches Herzzentrum München, Department of Anaesthesiology, Technische Universität München Recruiting
Munich, Bavaria, Germany, D-80636
Sponsors and Collaborators
Deutsches Herzzentrum Muenchen
Investigators
Principal Investigator: Patrick N Mayr, M.D. Deutsches Herzzentrum München, Department of Anaesthesiology, Technische Universität München
Principal Investigator: Peter Tassani, M.D., Ph.D Deutsches Herzzentrum München, Department of Anaesthesiology, Technische Universität München
Principal Investigator: Klaus Martin, M.D. Deutsches Herzzentrum München, Department of Anaesthesiology, Technische Universität München
Principal Investigator: Thomas Ried, M.D. Deutsches Herzzentrum München, Department of Anaesthesiology, Technische Universität München
  More Information

Responsible Party: N Patrick Mayr, MD, Deutsches Herzzentrum Muenchen
ClinicalTrials.gov Identifier: NCT01390675     History of Changes
Other Study ID Numbers: GE DHM-AN-OR-2011/04
GE DHM-AN-OR-2011/04 ( Other Identifier: Deutsches Herzzentrum München )
First Submitted: June 27, 2011
First Posted: July 11, 2011
Last Update Posted: July 26, 2017
Last Verified: August 2016

Additional relevant MeSH terms:
Heart Failure
Heart Arrest
Heart Diseases
Cardiovascular Diseases