clinical trial · NCT05829460
Primary Prevention and Uterine Preservation in Premenopausal Women With Obesity and Endometrial Hyperplasia
Endometrial HyperplasiaSemaglutidePlaceboLNG-IUD (Progestin)Telemedicine behavioral weight program
brief summary
The investigators hypothesize that combined treatment with the GLP-1R agonist semaglutide 2.4 mg and levonorgestrel intrauterine device (LNG-IUD), compared to LNG-IUD alone, will result in improved likelihood of uterine preservation, sustained weight loss, improved endometrial and metabolomic response to progestin, and improved quality of life in premenopausal women with endometrial hyperplasia who desire uterine preservation.
started
Mar 12, 2025
primary completion
Apr 30, 2030
completion
Apr 30, 2032
last updated
Jan 12, 2026
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol