30
Participants
Start Date
January 8, 2022
Primary Completion Date
December 30, 2024
Study Completion Date
June 30, 2026
levonorgestrel-releasing intrauterine system
Enrolled patients will be inserted this device for treating AEH to preserve fertility for 3-6 months or longer till complete response or operation if treatment fails, and the device may be removed if treatment changes.
Polyethylene Glycol Loxenatide
Initiate injection of Loxenatide will be 0.1mg per week, if the patient can tolerate, the dose will be increased to 0.2mg per week, or else 0.1mg per week will be injected and the injection will last for no more than 28 weeks. If the patient cannot tolerate the least 0.1mg/week, she must be excluded from this trial.
Obstetrics & Gynecology Hospital of Fudan University, Shanghai
Fudan University
OTHER