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Clinical Trial Summary

The primary purpose of this study is to compare residual ovarian function and therapeutic efficacy of surgical resection and catheter-directed sclerotherapy for ovarian endometrioma


Clinical Trial Description

Screening - History, Physical examination - Vital signs - Laboratory test (Serum AMH, CA-125, HE-4) / EKG / MRI - EHP-30 Intervention - Surgical enucleation or catheter-directed sclerotherapy - Laboratory test / EKG - Adverse event monitoring Follow-up visit #1 (1 month) - Vital signs - Lab test (AMH, CA-125) / Ultrasound - Adverse event monitoring Follow-up visit #2 (6 months) - Vital signs - Lab test (AMH, CA-125) / Ultrasound / Contrast-enhanced MRI - EHP-30 Follow-up visit #3 (12months) - Vital signs - Lab test (AMH, CA-125) / Ultrasound - EHP-30 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05279209
Study type Interventional
Source Yonsei University
Contact Kichang Han
Phone 82-10-9722-6315
Email wowsaycheese@yuhs.ac
Status Recruiting
Phase N/A
Start date December 18, 2021
Completion date December 17, 2023

See also
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