LivingGLP1
Study S001290

Semaglutide for the Treatment of Glucose Intolerance in Women With Prior Gestational Diabetes: a Double Blind RCT

Registration

Registration
NCT05569772
Acronym
SERENA
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
TRIPLE
Status
RECRUITING
Enrollment
252
Start
2023-09-14
Primary completion
2030-03
Lead sponsor
Universitaire Ziekenhuizen KU Leuven
Conditions
Glucose Intolerance After a Recent History of Gestational Diabetes
Interventions
DRUG:Semaglutide Pen Injector; DRUG:Semaglutide placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:2022-502082-22-00

Registered primary outcomes

  • Development of T2DM [by 160 weeks]

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
R0015468Semaglutide for prevention of type 2 diabetes in women with postpartum prediabetes after gestational diabetes: protocol for a Belgian multicentre double-blind randomised placebo-controlled trial.
Vanlaer Y, BMJ open
2026ProtocolPMID 42493207DOIcites ClinicalTrials.gov:NCT05569772; cites CTIS:2022-502082-22-00; registry reference RESULT:42493207