Progesterone and the premenstrual syndrome: a double blind crossover trial

British medical journal (Clinical research ed.), 290(6482), 1617-1621

DOI 10.1136/bmj.290.6482.1617 PMID 3924191 Source

Abstract

A double blind, randomised, crossover trial of oral micronised progesterone (two months) and placebo (two months) was conducted to determine whether progesterone alleviated premenstrual complaints. Twenty three women were interviewed premenstrually before treatment and in each month of treatment. They completed Moos's menstrual distress questionnaire, Beck et al's depression inventory, Spielberger et al's state anxiety inventory, the mood adjective checklist, and a daily symptom record. Analyses of data found an overall beneficial effect of being treated for all variables except restlessness, positive moods, and interest in sex. Maximum improvement occurred in the first month of treatment with progesterone. Nevertheless, an appreciably beneficial effect of progesterone over placebo for mood and some physical symptoms was identifiable after both one and two months of treatment. Further studies are needed to determine the optimum duration of treatment.

Topics

progesterone premenstrual syndrome treatment, pms progesterone supplementation trial, oral micronized progesterone pms, progesterone therapy premenstrual symptoms, pms mood symptoms progesterone, premenstrual disorder progesterone effectiveness, luteal phase progesterone pms relief, progesterone double-blind pms trial, premenstrual syndrome hormone treatment, progesterone mood improvement pms, pms physical symptoms progesterone, micronized progesterone premenstrual relief

Cite this article

Dennerstein, L., Spencer-Gardner, C., Gotts, G., Brown, J. B., Smith, M. A., & Burrows, G. D. (1985). Progesterone and the premenstrual syndrome: a double blind crossover trial. *British medical journal (Clinical research ed.)*, *290*(6482), 1617-1621. https://doi.org/10.1136/bmj.290.6482.1617

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