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Anesthesia for Catheter Aortic Valve ImplantATIOn Registry (AVIATOR)

This study is currently recruiting participants.
See Contacts and Locations
Verified August 2016 by N Patrick Mayr, Deutsches Herzzentrum Muenchen
Sponsor:
Information provided by (Responsible Party):
N Patrick Mayr, Deutsches Herzzentrum Muenchen
ClinicalTrials.gov Identifier:
NCT01390675
First received: June 27, 2011
Last updated: July 25, 2017
Last verified: August 2016
  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

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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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 )
Study First Received: June 27, 2011
Last Updated: July 25, 2017

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

ClinicalTrials.gov processed this record on August 22, 2017