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NCT03081676: HNF1A-Clamp

The Effect of GIP and GLP-1 on Insulin and Glucagon Secretion in Patients With HNF1A-diabetes Treated With or Without Sulphonylurea

Completed NA Last updated 27 June 2019
What this trial tests

NA trial testing Glimepiride 1Mg Tablet in Maturity-Onset Diabetes of the Young, Type 3 in 20 participants. Completed in 1 June 2018.

Timeline
8 March 2017
Primary endpoint
1 June 2018
1 June 2018

Quick facts

Lead sponsorUniversity Hospital, Gentofte, Copenhagen
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposebasic science
Enrollment20
Start date8 March 2017
Primary completion1 June 2018
Estimated completion1 June 2018
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

University Hospital, Gentofte, Copenhagen

Who can join

18 and older, any sex, with Maturity-Onset Diabetes of the Young, Type 3. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The most prevalent monogenetic diabetic subtype is named maturity onset diabetes of the young type (MODY3) or hepatocyte nuclear factor 1α (HNF1A)-diabetes. The aim of this study is to evaluate the effects of supra-physiological levels of GIP and GLP-1, respectively, on insulin and glucagon secretion at fasting plasma glucose (FPG) and "post-prandial" PG levels (1.5 × FPG) in patients with HNF1A-diabetes and matched healthy controls treated with or without a low dose of glimepiride (sulphonylurea). In addition, we will evaluate the maximal insulin and glucagon secretory capacity in both groups.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. GIP and GLP-1 Potentiate Sulfonylurea-Induced Insulin Secretion in Hepatocyte Nuclear Factor 1α Mutation Carriers.
    Christensen AS, Hædersdal S, Storgaard H, Rose K, et al · · 2020 · cited 18× · PMID 32518064 · DOI 10.2337/db20-0074

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