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Clinical Trial Summary

The investigators' objective is to determine the regression rate, side effects and acceptability of Mirena compared to megace in the treatment of atypical endometrial hyperplasia among women desiring fertility.


Clinical Trial Description

Atypical endometrial hyperplasia is a growing clinical problem that increases the risk of carcinogenesis and negatively impacts fertility. Although oral medical treatment may lead to regression in up to 90% of patients, they are associated with adverse side effects such as weight gain, that negatively affects fertility. To-date, there has been no RCTs evaluating the performance of the Mirena Intrauterine System (IUS) with megestrol acetate (megace) (the most effective and commonly used progestogen) in treating women with atypical hyperplasia who still desire fertility. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05492487
Study type Interventional
Source KK Women's and Children's Hospital
Contact Jessie Phoon, Dr
Phone 98242158
Email jessie.phoon.w.l@singhealth.com.sg
Status Recruiting
Phase Phase 2
Start date January 3, 2020
Completion date March 31, 2023

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