Progestin (Progesterone-Like Hormones) Induced Dysphoria (Depressed Mood, Irritability, Anxiety)

Sponsor
National Institute of Mental Health (NIMH) (NIH)
Overall Status
Completed
CT.gov ID
NCT00001770
Collaborator
(none)
50
1
60
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Study Details

Study Description

Brief Summary

Often women are prescribed hormone replacement therapy (HRT) during the perimenopause or menopause.

Hormone replacement therapy includes both estrogen and progesterone. The estrogen component of HRT helps to relieve the symptoms and has a beneficial effect on the heart and bones, but estrogen also increases the risk of uterine cancer. The progesterone component of the HRT (progestin) works to prevent the increased risk of uterine cancer.

There is evidence that some women experience unpleasant mood symptoms (such as irritability, depressed mood and anxiety) while receiving hormone replacement therapy (HRT) while taking the progestin / progesterone component of the HRT.

This study is designed to evaluate the ability of progestins to produce negative mood symptoms in women. Researchers intend on doing this by comparing the effects of medroxyprogesterone acetate (Provera) and a placebo inactive sugar pill. Patient's moods will be monitered based on their response to questionnaires answered in the outpatient clinic and at home.

This research will attempt to answer the following questions:
  1. Are progestins associated with changes in mood during hormone replacement therapy?

  2. If progestins are associated with mood disturbance, is it because they are blocking the beneficial effects of estrogen?

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    There is evidence in the literature that some women experience dysphoric symptoms while receiving hormone replacement therapy (HRT) and that this disturbance in mood is related to the progestin component of the HRT. The bulk of this evidence is anecdotal. While some authors have attempted to examine this putative problem in a more systematic fashion, there are no controlled studies that attempt to identify the mechanism through which the perturbation in mood occurs. Adverse effects of progestins might be mediated directly through the progesterone or androgen receptor. Alternatively, the effects of progestins might be consequent to the antiestrogen effects of progesterone. This latter possibility is in part supported by our observation in previous studies of the beneficial effects of estradiol on mood and the possible precipitation of mood disturbance following acute estrogen withdrawal. Finally, despite the popular lore that progesterone causes mood disturbances, a placebo effect cannot be ruled out, since women taking HRT know when they are receiving the progestin component of the regimen. Our research questions therefore are as follows: 1) Are progestins associated with changes in mood during HRT, and 2) If progestins are associated with mood disturbance, is it because they are blocking the beneficial effects of estrogen?

    Study Design

    Study Type:
    Observational
    Official Title:
    The Phenomenology and Biophysiology of Progestin-Induced Dysphoria
    Study Start Date :
    Mar 1, 1998
    Study Completion Date :
    Mar 1, 2003

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      N/A and Older
      Sexes Eligible for Study:
      Female
      Accepts Healthy Volunteers:
      Yes

      INCLUSION CRITERIA

      The subjects in this study will be women who meet the following criteria:
      1. history of mood and/or behavioral symptoms associated with hormone replacement therapy;

      2. age 40 to 65;

      3. in good medical health.

      EXCLUSION CRITERIA

      Any subject with significant physical, EKG, mammogram or laboratory abnormalities will not participate in this protocol. Additionally prior to participation all subjects will be examined for any contradictions to estrogen therapy (as determined by a pelvic exam and mammogram) within the past year by a gynecologist of their choice. In those patients who are unable to independently arrange this exam, we have arranged for a consultant gynecologist to be available through our collaboration with NICHD.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 National Institute of Mental Health (NIMH) Bethesda Maryland United States 20892

      Sponsors and Collaborators

      • National Institute of Mental Health (NIMH)

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00001770
      Other Study ID Numbers:
      • 980079
      • 98-M-0079
      First Posted:
      Nov 4, 1999
      Last Update Posted:
      Mar 4, 2008
      Last Verified:
      Mar 1, 2003

      Study Results

      No Results Posted as of Mar 4, 2008