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Band to Bypass - Metabolism Kinetics in Gastric Bypass and Banding

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified March 2012 by Hvidovre University Hospital.
Recruitment status was:  Recruiting
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
  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   (Adult)
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01559792

Locations
Denmark
Hvidovre Hospital
Hvidovre, Denmark, 2650
Sponsors and Collaborators
Hvidovre University Hospital
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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 December 05, 2016