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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00908973
Other study ID # RnonR
Secondary ID
Status Completed
Phase N/A
First received May 26, 2009
Last updated March 19, 2012
Start date May 2009
Est. completion date December 2011

Study information

Verified date March 2012
Source Hvidovre University Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection AgencyDenmark: The Regional Committee on Biomedical Research Ethics
Study type Observational

Clinical Trial Summary

The aim of the study is to describe differences in meal-stimulated gut hormone response, appetite and intestinal transit time between good and poor responders 1-2 years after Gastric Bypass surgery for obesity.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date December 2011
Est. primary completion date June 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- Age 20-60 years

- Completed laparoscopic gastric bypass surgery without complications (cases)

- No previous gastric bypass surgery (controls)

Exclusion Criteria:

- Diabetes

- Disease or treatment interfering with appetite or gastrointestinal motility

- Pregnancy or breastfeeding

- Excess weight loss 1 year after gastric bypass > 50% and =< 60% (cases)

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Department of Endocrinology at Hvidovre University Hospital Hvidovre Copenhagen

Sponsors (3)

Lead Sponsor Collaborator
Hvidovre University Hospital Novo Nordisk A/S, University of Copenhagen

Country where clinical trial is conducted

Denmark, 

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