LivingGLP1
Study S000334

The Impact of Pramlintide on Top of Semaglutide in Obese People With Prediabetes

Registration

Registration
NCT06619015
Acronym
TOTT
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2; PHASE3
Masking
TRIPLE
Status
WITHDRAWN
Enrollment
0
Start
2025-04-01
Primary completion
2025-04-01
Lead sponsor
Esbjerg Hospital - University Hospital of Southern Denmark
Conditions
Obesity; Appetite Regulation; PreDiabetes
Interventions
DRUG:Pramlintide Acetate 1 MG/ML; DRUG:Semaglutide Pen Injector; DRUG:Sodium Chloride 0.9% Inj
Results posted
FALSE
Secondary identifiers
CTIS:2024-510802-10-00

Registered primary outcomes

  • Change in kilocalorie (kCal) consumption at ad libitum meal test, from baseline, to after 26 weeks of semaglutide of which the last two weeks is with the addition of either pramlintide or placebo [From baseline at the start of the study(week 0), to the end of the study after 26 weeks]

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