Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Markus Mueller, University of Zurich
ClinicalTrials.gov Identifier:
NCT00497627
First received: July 5, 2007
Last updated: July 8, 2013
Last verified: July 2013
  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 University of Zurich:

Primary Outcome Measures:
  • Quality of Life [ Time Frame: 2 to 5 years after debanding ] [ Designated as safety issue: No ]

Enrollment: 12
Study Start Date: January 2007
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Detailed Description:

Follow up of debanding patients regarding cardiometabolic risk factors

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
Please refer to this study by its ClinicalTrials.gov identifier: NCT00497627

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

No publications provided

Responsible Party: Markus Mueller, PD Dr. med., University of Zurich
ClinicalTrials.gov Identifier: NCT00497627     History of Changes
Other Study ID Numbers: StV 38-2006
Study First Received: July 5, 2007
Last Updated: July 8, 2013
Health Authority: Switzerland: Swissmedic

ClinicalTrials.gov processed this record on April 17, 2014