LivingGLP1
Study S001535

The Impact of Lixisenatide on Postprandial Glucose Tolerance in Pancreatectomised Subjects -a Delineation of Extrapancreatic Effects

Registration

Registration
NCT02640118
Acronym
Px-Lixi
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Status
COMPLETED
Enrollment
24
Start
2015-08
Primary completion
2016-07
Lead sponsor
University Hospital, Gentofte, Copenhagen
Conditions
Diabetes After Total Pancreatectomy
Interventions
DRUG:Lixisenatide; DRUG:Lixisenatide-Placebo; OTHER:Standardized liquid meal
Results posted
FALSE
Individual participant data sharing
UNDECIDED

Registered primary outcomes

  • PPG excursions measured as incremental area under curve (iAUC) [-120,-45,-30,-15,0,5,10,15,20,25,30,40,50,60,70,80,90,105,120,135,150,180 minutes]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0017361The GLP-1 receptor agonist lixisenatide reduces postprandial glucose in patients with diabetes secondary to total pancreatectomy: a randomised, placebo-controlled, double-blinded crossover trial.
Juel CTB, Diabetologia
2020Randomized trialPMID 32394228DOIcites ClinicalTrials.gov:NCT02640118; registry reference DERIVED:32394228