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Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00497627
First Posted: July 6, 2007
Last Update Posted: May 12, 2016
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. Read our disclaimer for details.
Collaborator:
Cantonal Hospital, Frauenfeld
Information provided by (Responsible Party):
Markus Mueller, University of Zurich
  Purpose
Follow up of debanding patients

Condition
Bariatric Patients

Study Type: Observational
Official Title: Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

Further study details as provided by Markus Mueller, University of Zurich:

Primary Outcome Measures:
  • Quality of Life [ Time Frame: 2 to 5 years after debanding ]

Enrollment: 12
Study Start Date: January 2007
Study Completion Date: February 2015
Primary Completion Date: January 2015 (Final data collection date for primary outcome measure)
Detailed Description:
Follow up of debanding patients regarding cardiometabolic risk factors
  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:   Non-Probability Sample
Study Population
Follow up of debanding patients regarding cardiometabolic risk factors
Criteria

Inclusion criteria:

  • Previous debanding after lap. gastric bypass

Exclusion criteria:

  • Further bariatric procedures
  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): NCT00497627


Locations
Switzerland
University Hospital of Zurich
Zurich, Switzerland
Sponsors and Collaborators
University of Zurich
Cantonal Hospital, Frauenfeld
Investigators
Study Director: 01 Studienregister MasterAdmins UniversitaetsSpital Zuerich
  More Information

Responsible Party: Markus Mueller, PD Dr. med., University of Zurich
ClinicalTrials.gov Identifier: NCT00497627     History of Changes
Other Study ID Numbers: StV 38-2006
First Submitted: July 5, 2007
First Posted: July 6, 2007
Last Update Posted: May 12, 2016
Last Verified: May 2016