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Join the Endo-Epic Study

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About The Study

The Endo-Epic Study (Endometriosis Estradiol-Mediated Pain, Inflammation, and Central Sensitization Study) is designed to explore how a hormone-suppressing medication, relugolix combination-therapy (Relugolix CT), may influence pelvic pain, inflammation, and sensitivity to pain in premenopausal women who have moderate-to-severe endometriosis-associated pelvic pain.

Participants in this study will take part in a 28-week research program, which includes a 24-week period of receiving Relugolix CT (Myfembree®) — a medication approved by the U.S. Food and Drug Administration for the treatment of moderate-to-severe pain associated with endometriosis. Throughout the study, participants will complete a combination of in-person and virtual visits, including brief online surveys to assess symptoms, monthly urine pregnancy tests, and specialized tests such as MRI imaging and pain sensitivity (sensory) evaluations.

Through this research, investigators aim to learn more about the biological and hormonal factors that contribute to pelvic pain in endometriosis, with the hope of informing future treatment strategies and improving quality of life for those affected.

Quick Facts

Local Study

Includes four full-day in-person visits in Ann Arbor, MI.

Combination-Therapy Research

Participants will receive relugolix CT (Myfembree®) during the study at no cost.

For Premenopausal Women

Women aged 21 - 49 who have endometriosis diagnosed by surgery, ultrasound, or MRI.

Compensation Provided

Participants will be compensated up to $1,345 for their time and effort.

Who Can Participate?
  • Premenopausal females aged 21–49
  • Endometriosis diagnosed by surgery, pelvic ultrasound, or MRI (within 5 years)
  • Moderate-to-severe pelvic pain for at least 6 months
  • Able to read and speak English
  • Willing to be off all hormonal medications for 30–60 days before starting study medication
  • Willing and eligible to use Relugolix CT for at least 6 months
  • Willing and eligible to undergo brain MRI, sensory testing, and other study procedures
  • No history of hysterectomy
  • No history of blood clots; uncontrolled high blood pressure; diabetes with organ damage; certain severe migraines; breast cancer or hormone-sensitive cancer; osteoporosis; undiagnosed vaginal bleeding; liver problems

What to Expect:

28-week participation. 24-week period receiving Relugolix CT
9 total study visits (4 in-person, 5 phone/virtual)
Bone density scan to confirm eligibility (provided at no cost)
Monthly urine pregnancy tests
Online surveys about pain, bleeding, fatigue, and medication use
Brain MRI and sensory testing as part of study procedures

Compensation & Benefits:

Participants will be compensated up to $1,345 for their time and effort over the course of the study. This compensation acknowledges the time spent completing study visits, participating in tests and imaging, and engaging in follow-up assessments.
All study-related care, medication, and procedures — including MRI, and laboratory evaluations — are provided at no cost to participants.
Our goal is to ensure that participation is accessible, supported, and respectful of each individual’s time and contribution to advancing women’s health research.

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SEE IF YOU QUALIFY

We’ve pulled together some basics to help you

What is the purpose of this study?

The study is designed to better understand how hormone suppression with relugolix combination-therapy affects pain, inflammation, and pain sensitivity in women with endometriosis-related pelvic pain.

Where do study visits take place?

Four in-person visits will take place in Ann Arbor, Michigan. Additional visits may occur virtually or by phone.

What does participation involve?

Participation includes surveys, pregnancy testing, MRI, sensory testing, and taking relugolix CT for 24 weeks, with nine total visits over 28 weeks.

Is there any cost to join?

No. Study medication and all study tests are provided at no cost. Compensation is provided for participation.