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Clinical Trial Summary

Using the glucagon-like peptide-1 (GLP-1) antagonist exendin(9-39) and the glucose-dependent insulinotropic peptide (GIP) antagonist GIP(3-30), the purpose of this study is to clarify the importance of endogenous GLP-1 and GIP for postprandial glucose metabolism after RYGB and SG in subjects with normal glucose tolerance. We hypothesize that GLP-1 is more important after RYGB, and GIP is more important after SG, for postprandial glucose tolerance and beta-cell function. A group of un-operated subjects with normal glucose tolerance will serve as controls.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03950245
Study type Interventional
Source Hvidovre University Hospital
Contact
Status Completed
Phase N/A
Start date July 1, 2019
Completion date April 16, 2021

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