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Clinical Trial Summary

The purpose of this study is to compare the efficacy of the vaginal micronized progesterone and Levonorgestrel-releasing Intrauterine System for treatment of non-atypical endometrial hyperplasia in premenopausal women.


Clinical Trial Description

Vaginal use of micronized progesterone in the treatment of endometrial hyperplasia can result in better than oral administration, as it will remain away from the first pass effect, and depending on the local application. In this study, we aimed to compare this local treatment with Levonorgestrel-releasing Intrauterine System for treatment of non-atypical endometrial hyperplasia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03992937
Study type Interventional
Source Kocaeli University
Contact
Status Completed
Phase N/A
Start date June 20, 2019
Completion date December 1, 2020

See also
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Not yet recruiting NCT06378489 - The Use of Etonogestrel Contraceptive Implant as Treatment for Endometrial Hyperplasia Without Atypia: A Cohort Study
Completed NCT01685762 - Metformin for the Treatment of Endometrial Hyperplasia Early Phase 1
Completed NCT03675139 - MPA Versus Dydrogesterone for Management of Endometrial Hyperplasia Without Atypia Phase 3