Review: progesterone or progesterone lead to a marginal reduction in premenstrual syndrome symptoms.
نویسنده
چکیده
Main results 10 studies (531 women) of 14 published trials testing the efficacy of progesterone met the selection criteria. 1 study used both suppositories and oral preparations and was treated as 2 studies in the meta-analysis. The pooled results for 8 studies on suppositories and 3 studies on oral drugs showed a small benefit for progesterone in the reduction of symptoms (table). When results were analysed according to route of administration, a small benefit in favour of placebo over suppositories and in favour of oral micronised progesterone over placebo were seen (table). 3 studies (4 comparisons) of 15 published trials comparing progestogens with placebo met the selection criteria. The progestogens were medroxyprogesterone, 15 mg (1 study); norethisterone, 15 mg (1 study); and dydrogesterone, 20 mg (2 studies). The pooled results showed a marginal benefit for progestogens over placebo in the reduction of symptoms (table). The difference in withdrawals resulting from side effects was not statistically significant for progesterone or progestogens (table).
منابع مشابه
Efficacy of progesterone and progestogens in management of premenstrual syndrome: systematic review.
OBJECTIVE To evaluate the efficacy of progesterone and progestogens in the management of premenstrual syndrome. DESIGN Systematic review of published randomised, placebo controlled trials. STUDIES REVIEWED 10 trials of progesterone therapy (531 women) and four trials of progestogen therapy (378 women). MAIN OUTCOME MEASURES Proportion of women whose symptoms showed improvement with proges...
متن کاملProgesterone, fluid, and electrolytes in premenstrual syndrome.
Changes in mood, plasma progesterone concentration, urinary volume, sodium excretion, sodium:potassium ratio, and body weight during the menstrual cycle were determined in 18 women with premenstrual syndrome and 10 symptomless (control group) women. Plasma progesterone concentration was higher in the women with symptoms during the postovulatory phase of the cycle, and the peak progesterone conc...
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Objective: The aim was to investigate the effect on mood and the physical symptoms of two dosages of natural progesterone and a placebo in postmenopausal women with and without a history of premenstrual syndrome (PMS). Design: A randomized, placebo-controlled, double-blind, crossover study was performed. Method: Postmenopausal women ðn 1⁄4 36Þ with climacteric symptoms were recruited. They rece...
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Premenstrual syndrome is defined as recurrent moderate psychological and physical symptoms that occur during the luteal phase of menses and resolve with menstruation. It affects 20 to 32 percent of premenopausal women. Women with premenstrual dysphoric disorder experience affective or somatic symptoms that cause severe dysfunction in social or occupational realms. The disorder affects 3 to 8 pe...
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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. Department ofPsychiatry, University ofMelbourne, Austin Hospital L DENNERSTEIN, FRANzcP, PHD, psych...
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عنوان ژورنال:
- Evidence-based mental health
دوره 5 2 شماره
صفحات -
تاریخ انتشار 2002