Moderate to Severe
Endometriosis-Related Pain or Heavy Menstrual Bleeding from Uterine Fibroids?
Consider participating in a clinical trial studying bone safety of an FDA approved treatment!
Call Us: (385) 695-2300
or activate the QR code below to inquire about participating
Moderate to Severe
Endometriosis-Related Pain or Heavy Menstrual Bleeding from Uterine Fibroids?
Consider participating in a clinical trial studying bone safety of an FDA approved treatment!
Call Us: (385) 695-2300
or activate the QR code below to inquire about participating
Criteria:
To qualify, participants in this study will be women who:
- Are from 18 to 50 years old and premenopausal
Have a formal diagnosis of Endometriosis (with imaging OR clinical documentation) and suffer from moderate to severe pain both during menses and off menses,
OR
Have a formal diagnosis of Uterine Fibroids (with clinical documentation or imaging) and suffer from heavy menstrual bleeding.
Are willing to avoid pregnancy for 4 years during treatment using non-hormonal contraception.
Agree to a study-provided DXA Bone Density Scan throughout 4 years of treatment and 1 year of post-treatment follow up.
If you are eligible, you will receive study medicine and study-related care at no cost to you and may be compensated for time and transportation.
Contact us for more information and to see if you qualify. Why not be a part of the conversation when it comes to the future of your treatment options?
Study Location
Physicians’ Research Options, LLC®
11724 South State Street – Suite 201
Draper, Utah 84020
d.pessetto.crc@proslc.com
385.695.2300 Site
801.664.4471 Cell/Text
www.proslc.com
About PRO
Physicians’ Research Options (PRO) is an experienced Clinical Research Company dedicated to the performance of Phase II, III and IV Pharmaceutical and Pilot/Pivotal Medical Device clinical trials. Our staff experience totals over 60 years in Clinical / Medical Research.
Our staff recruits for and manages studies in Utah and Colorado.
