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Band to Bypass - Metabolism Kinetics in Gastric Bypass and Banding

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ClinicalTrials.gov Identifier: NCT01559792
Recruitment Status : Unknown
Verified March 2012 by Siv Hesse Jacobsen, Hvidovre University Hospital.
Recruitment status was:  Recruiting
First Posted : March 21, 2012
Last Update Posted : March 21, 2012
Sponsor:
Information provided by (Responsible Party):
Siv Hesse Jacobsen, Hvidovre University Hospital

Brief Summary:
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 or disease
Gastric Bypass Gastric Banding

Study Type : Observational
Estimated Enrollment : 18 participants
Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Gastric Banding to Bypass - Metabolism Kinetics in Gastric Bypass and Banding
Study Start Date : December 2011
Estimated Primary Completion Date : December 2012



Biospecimen Retention:   Samples With DNA
blood


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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