Intrauterine Device Versus Uterine Artery Embolization for Adenomyosis

Status Recruiting

Clinical Trial Summary

The primary purpose of this study is to compare the therapeutic efficacy of intrauterine device and uterine artery embolization for uterine adenomyosis.

Clinical Trial Description

Screening - History, Physical examination - Laboratory test (Hemoglobin) / MRI - Pictorial blood loss assessment chart - Symptom/Quality of life score Intervention - Intrauterine device or uterine artery embolization - Adverse event montoring Follow-up visit #1 (1 month) - Vital signs - blood test (Hemoglobin) / Ultrasound - Adverse event monitoring Follow-up visit #2 (3 month) • MRI only for embolization patients Follow-up visit #3 (6 months) - Blood test (Hemoglobin) / Ultrasound - Pictorial blood loss assessment chart - Symptom/Quality of life score Follow-up visit #4 (12months) - Blood test (Hemoglobin) / Ultrasound - Pictorial blood loss assessment chart - Symptom/Quality of life score ;

Study Design

Related Conditions & MeSH terms

Adenomyosis

Clinical Trial Details

NCT number	NCT06043583
Study type	Interventional
Source	Yonsei University
Contact	Man-Deuk Kim
Phone	82-10-8625-2197
Email	mdkim@yuhs.ac
Status	Recruiting
Phase	N/A
Start date	July 21, 2023
Completion date	July 2025

View Details

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