Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

Bariatric Patients Clinical Trial

Official title:

Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00497627
• Other study ID #: StV 38-2006
• Status: Completed
• Phase: N/A
• First received: July 5, 2007
• Last updated: May 11, 2016
• Start date: January 2007
• Est. completion date: February 2015

Study information

• Verified date: May 2016
• Source: University of Zurich
• Contact: n/a
• Is FDA regulated: No
• Health authority: Switzerland: Swissmedic
• Study type: Observational

Clinical Trial Summary

Follow up of debanding patients

Description:

Follow up of debanding patients regarding cardiometabolic risk factors

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: February 2015
• Est. primary completion date: January 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion criteria:

• Previous debanding after lap. gastric bypass

Exclusion criteria:

• Further bariatric procedures

Study Design

N/A

Related Conditions & MeSH terms

• Bariatric Patients

Locations

Country	Name	City	State
Switzerland	University Hospital of Zurich	Zurich

Sponsors (2)

Lead Sponsor	Collaborator
University of Zurich	Cantonal Hospital, Frauenfeld

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quality of Life		2 to 5 years after debanding	No