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Band to Bypass - Metabolism Kinetics in Gastric Bypass and Banding

This study is currently recruiting participants.
Verified March 2012 by Hvidovre University Hospital
Sponsor:
Information provided by (Responsible Party):
Siv Hesse Jacobsen, Hvidovre University Hospital
ClinicalTrials.gov Identifier:
NCT01559792
First received: March 19, 2012
Last updated: March 20, 2012
Last verified: March 2012
History of Changes
  Purpose

The investigators want to study the changes in secretion of gastrointestinal hormones, absorption and metabolism of food and liquids before and after gastric bypass and in patients who are gastric banded but are getting conversion to a gastric bypass. All patients are with normal glucose tolerance. The investigators hypothesis that food uptake/absorption of food is faster after gastric bypass and the secretion of gastrointestinal hormones change.


Condition
Gastric Bypass
Gastric Banding

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Gastric Banding to Bypass - Metabolism Kinetics in Gastric Bypass and Banding

Further study details as provided by Hvidovre University Hospital:

Biospecimen Retention:   Samples With DNA

blood


Estimated Enrollment: 18
Study Start Date: December 2011
Estimated Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

all with normal glucose tolerance - patients who are undergoing gastric bypass and patients with a gastric band to are converted to gastric bypass

Criteria

Inclusion Criteria:

  • Normal glucose tolerance
  • Patients who are undergoing gastric bypass and patients with a gastric band to are converted to gastric bypass

Exclusion Criteria:

  • Diabetes,
  • Study population must undergo gastric bypass
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01559792

Contacts
Contact: siv H Jacobsne, MD +4538626357 siv.hesse@hotmail.com

Locations
Denmark
Hvidovre Hospital Recruiting
Hvidovre, Denmark, 2650
Contact: Siv H Jacobsen            
Principal Investigator: Siv H Jacobsen, MD            
Hvidovre hospital Recruiting
Hvidovre, Denmark, 2650
Contact: siv H Jacobsen, MD            
Sponsors and Collaborators
Hvidovre University Hospital
  More Information

No publications provided

Responsible Party: Siv Hesse Jacobsen, MD, Hvidovre University Hospital
ClinicalTrials.gov Identifier: NCT01559792     History of Changes
Other Study ID Numbers: BG092011
Study First Received: March 19, 2012
Last Updated: March 20, 2012
Health Authority: Denmark: Danish Dataprotection Agency
Denmark: Ethics Committee

ClinicalTrials.gov processed this record on May 23, 2013