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Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2007 by University of Zurich.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
University of Zurich
ClinicalTrials.gov Identifier:
NCT00497627
First received: July 5, 2007
Last updated: NA
Last verified: July 2007
History: No changes posted
  Purpose

Follow up of debanding patients


Condition
Bariatric Patients

Study Type: Observational
Study Design: Additional Descriptors: Psychosocial
Observational Model: Defined Population
Time Perspective: Cross-Sectional
Time Perspective: Retrospective
Official Title: Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

Further study details as provided by University of Zurich:

Enrollment: 12
Study Start Date: January 2007
Estimated Study Completion Date: August 2007
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
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

ClinicalTrials.gov Identifier: NCT00497627     History of Changes
Other Study ID Numbers: StV 38-2006
Study First Received: July 5, 2007
Last Updated: July 5, 2007
Health Authority: Switzerland: Swissmedic

ClinicalTrials.gov processed this record on May 16, 2013