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

PHASE2RecruitingINTERVENTIONAL
Enrollment

96

Participants

Timeline

Start Date

March 12, 2025

Primary Completion Date

April 30, 2030

Study Completion Date

April 30, 2032

Conditions
Endometrial Hyperplasia
Interventions
DRUG

Semaglutide

This medication is self-administered as a subcutaneous injection in the abdomen, thigh, or upper arm; injection site should be rotated when using the same body region.

DRUG

Placebo

This medication is self-administered as a subcutaneous injection in the abdomen, thigh, or upper arm; injection site should be rotated when using the same body region.

DRUG

LNG-IUD (Progestin)

Released via the levonorgestrel-releasing IUD.

BEHAVIORAL

Telemedicine behavioral weight program

Optional to attend.

Trial Locations (1)

63110

RECRUITING

Washington University School of Medicine, St Louis

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Novo Nordisk A/S

INDUSTRY

lead

Washington University School of Medicine

OTHER

NCT05829460 - Primary Prevention and Uterine Preservation in Premenopausal Women With Obesity and Endometrial Hyperplasia | Biotech Hunter | Biotech Hunter