As someone whose been on a long term high dose of progesterone and having some gynaecological issues of late, I found this article interesting.
I'm going to be asking for a mri and scan at the hospital later this month.
Researchers at the National Institutes of Health's National Institute of Child Health and Human Development (NICHD) are evaluating a new treatment for women suffering from uterine fibroids: an experimental drug that blocks progesterone, a female sex hormone secreted by the ovaries. Because fibroids grow in response to progesterone, therapies that lower progesterone levels could cause fibroids to shrink. That could help relieve pain and other symptoms and possibly improve fertility in women with fibroids.
Currently there is only one effective hormone-reducing therapy available for relieving fibroid symptoms, but it has serious side effects. It works by blocking the master reproductive hormone, gonadotropin releasing hormone (GnRH). Blocking GnRH not only shuts down the body's production of progesterone. It also shuts down production of estrogen, another sex hormone. Since abruptly depriving the body of estrogen causes hot flashes and prolonged estrogen deprivation can weaken bones, this treatment can only be used short-term.
The NIH researchers hope to develop a therapy that would block progesterone while leaving estrogen alone. In theory, such a treatment could shrink fibroids but spare women from hot flashes and bone weakening. Lynnette Nieman and her NIH coworkers are seeking volunteers for their study of the drug, called CDB-2914, which prevents progesterone from acting in the tissues but which does not interfere with estrogen action. The study will evaluate whether this drug causes fibroids to shrink in pre-menopausal women. Prospective volunteers must
Be between 33 and 50 years old
Have regular menstrual cycles
Have a history of uterine fibroids that cause heavy bleeding, pressure, or pain.
After some preliminary medical tests, volunteers will receive either CDB-2914 or a placebo (an inactive compound) for three menstrual cycles. (Which option a woman receives is randomly assigned.) At the end of the treatment period, volunteers can choose one of several options: to receive a hysterectomy (surgery to remove the uterus) or a myomectomy (surgery where fibroids are removed but the uterus stays intact), or to receive three months of CDB-2914, regardless of whether or not they received it during the study. They can also choose to exit the study completely at that time.
To find out more about the study, call the NIH Patient Recruitment and Public Liaison Office at 1-800-411-1222. The e-mail address is
[email protected]. Information about the study is also available from
http://fibroids.nichd.nih.go