LivingGLP1
Study S001249

Primary Prevention and Uterine Preservation in Premenopausal Women With Obesity and Endometrial Hyperplasia

Registration

Registration
NCT05829460
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
WITHDRAWN
Enrollment
0
Start
2025-03-12
Primary completion
2030-04-30
Lead sponsor
Washington University School of Medicine
Conditions
Endometrial Hyperplasia
Interventions
DRUG:Semaglutide; DRUG:Placebo; DRUG:LNG-IUD (Progestin); BEHAVIORAL:Telemedicine behavioral weight program
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Number of patients with endometrial hyperplasia free biopsy with uterine preservation [At 2 years (or exit from study)]

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