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: (720) 382-1837
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: (720) 382-1837
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®
255 Union Blvd., Suite 200
Lakewood, CO 80228
d.kurz.ccrp@proslc.com
Janell.degiorgio.ccrc@proslc.com
720.382.1837 Site
303.284.0506 Fax
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.
