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Clinical Trails at Rush Premenstrual Dysphoric Disorder
Clinical Trial Protocol ID
05102702

Clinical Trial Investigator Name
Ann S. Hartlage

Clinical Trial Title

Inhibin B as a marker for premenstrual dysphoric disorder



Clinical Trial Protocol Description

Premenstrual dysphoric disorder (PMDD) is one of the most common conditions affecting women of reproductive age having a high impact on personal well-being and professional productivity. The purpose of this study is to explore the relationship between inhibin B, a new marker of ovarian function, and PMDD. Participation in the study includes a short orientation at Rush University Medical Center in Chicago, a physical examination including lab work (paid for by the study), an emotional health history interview, completion of a daily questionnaire for two menstrual cycles, at least three blood draws during each menstrual cycle (a phlebotomist can come to your home), and in-home ovulation testing.
Women who complete the study will receive $100.



Clinical Trial Eligibility Criteria

You may be eligible to participate in this study if you:

  • Are a Hispanic, black or white woman 18 to 53 years of age with regular menstrual cycles
  • Currently have premenstrual syndrome (PMS) or premenstrual dysphoric disorder (PMDD)
  • Are not taking hormones, including oral birth control pills
  • Are not taking a prescribed medication for an emotional or nervous problem

This is a partial list of eligibility requirements. To inquire about your eligibility, please call the contact number provided. If you wish to inquire via e-mail, please include the title of the study in your message.

 





Contact Name Karen Neimanas
Contact Phone (312) 563-2595
Contact E-mail clinical_trials@rush.edu
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Premenstrual Dysphoric Disorder

   
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