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Effect of Humulus lupulus L. (Hop) on Postmenopausal Sexual Dysfunction: A Randomized Clinical Trial.
Vahedpoorfard, Zahra; Ferdosi, Samira; Rahimi, Habibollah; Motedayyen, Hossein.
Affiliation
  • Vahedpoorfard Z; Autoimmune Diseases Research Center, Kashan University of Medical Sciences, Kashan, Iran.
  • Ferdosi S; Department of Obstetrics and Gynecology, Kashan University of Medical Sciences, Kashan, Iran.
  • Rahimi H; Department of Biostatics and Epidemiology, School of Public Health, Kashan University of Medical Sciences, Kashan, Iran.
  • Motedayyen H; Autoimmune Diseases Research Center, Kashan University of Medical Sciences, Kashan, Iran.
Int J Clin Pract ; 2023: 9528335, 2023.
Article in En | MEDLINE | ID: mdl-37101856
ABSTRACT

Objective:

Female sexual dysfunction is a common distressing problem among women, which may result from reducing circulating endogenous estrogen. Humulus lupulus L. (hop) has antioxidant, anti-inflammatory, anticancer, and estrogenic properties. Therefore, this study aimed to assess the efficacy of hop on postmenopausal sexual dysfunction.

Methods:

In the current randomized clinical trial, study populations consisted of 63 postmenopausal women who were randomly categorized into two groups. In the hop group (N = 33), women received the vaginal gel containing Hop extract every day for seven days and then continued for two months, twice weekly. In the estradiol group (N = 30), women were treated with vaginal estradiol (0.625 mg) over two 28-day cycles (21 days of therapy and seven days rest). The sexual function was evaluated using the Female Sexual Function Index (FSFI) questionnaire before and after intervention.

Results:

No statistically significant differences in FSFI scores (sexual desire, sexual arousal, vaginal lubrication, satisfaction, orgasm, sexual pain, and total FSFI) (P > 0.05) were noticed after treatment between the hop and estradiol groups.

Conclusion:

Vaginal hop was as effective as estradiol in improving the sexual dysfunction among postmenopausal women with no adverse events. This trial is registered with IRCT20210405050859N1.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sexual Dysfunction, Physiological / Humulus Type of study: Clinical_trials Limits: Female / Humans Language: En Journal: Int J Clin Pract Journal subject: MEDICINA Year: 2023 Type: Article Affiliation country: Iran

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sexual Dysfunction, Physiological / Humulus Type of study: Clinical_trials Limits: Female / Humans Language: En Journal: Int J Clin Pract Journal subject: MEDICINA Year: 2023 Type: Article Affiliation country: Iran