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Surgical Myomectomy Followed by Oral Myfembree Versus Standard of Care Trial (SOUL) — SOUL  

Pelvic Pain Clinical Trial

Official title:
Surgical Myomectomy Followed by Oral Myfembree Versus Standard of Care Trial.

Clinical Trial Summary

In this project, the proposition is that the use of daily dosed Myfembree ( a combination of relugolix with estradiol and norethindrone acetate), FDA-approved medication to treat heavy menses fibroid-related symptoms, has the potential to delay the recurrence of fibroid symptoms, prolong the improved quality of life and delay the need for re-intervention after uterine sparing surgery versus the routine standard of care.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05538689
Study type Interventional
Source University of Chicago
Contact Obianuju Sandra Madueke Laveaux, MD MPH
Phone (773) 834-7726
Email slaveaux@bsd.uchicago.edu
Status Recruiting
Phase Phase 4
Start date November 20, 2022
Completion date April 2026
View Details
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