Clinical Trials

Uterine Fibroid Study

Posted on 7/25/2017

The purpose of this study is to test how effective and safe the investigational study drug, given with and without FDA approved low-dose estradiol (estrogen) and norethindrone (progesterone) is in treating uterine fibroids and heavy menstrual bleeding.  The low dose estrogen and progesterone medication has been approved by the FDA as hormone replacement therapy to prevent bone loss. The use of the FDA approved low-dose estradiol and norethindrone used with the study drug to treat patients with heavy menstrual bleeding associated with uterine fibroids is investigational.

We want to find out if the study drug has an effect on the monthly menstrual blood loss, and pain associated with uterine fibroids as well as any effect on the size of the fibroids.

You may qualify if you:

  • have heavier than normal bleeding during your menstrual period
  • have been diagnosed with uterine fibroids or suspect uterine fibroids
  • are a premenopausal female aged 18 - 50 (inclusive)
If you qualify and complete all visits, you may receive up to $1,150 compensation for your time and travel while in the study.

Call for more information and to see if you qualify for a screening visit.  When you call, ask to speak to Kim.
What Our Research Patients are Saying
"I was on edge when I first went to DCOL Research because of the sensitive nature of my diagnosis. Upon arrival to the research office I was treated very kindly and professionally as soon as I signed in. The Research Coordinator was friendly and compassionate and made me feel at ease. I was informed about the trial and they ensured that I had a clear understanding of the information. During all my visits I felt at ease and informed. The Research Coordinator is very professional as is the Lab Coordinator. It is always a smooth process and the staff is confident and friendly. The study doctor is also helpful and always asks if I have any problems or concerns, just like the staff."

~ Anonymous

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