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Effects of Lepidium Meyenii Walp on Sexual Function in Postmenopausal Women

Phase 1
Conditions
Sexual Dysfunction, Physiological
Interventions
Behavioral: The Female Sexual Function Index (FSFI)
Behavioral: The Female Intervention Efficacy Index (FIEI)
Behavioral: The Beck Depression Inventory II
Drug: Placebo
Drug: Lepidium Meyenii Walp
Registration Number
NCT02624648
Lead Sponsor
Universidade do Vale do Sapucai
Brief Summary

Objective: To study the effects of Lepidium Meyenii in sexual function of postmenopausal women.

Method: It will be held a clinical, prospective, randomized, double-blind, placebo-controlled study with 144 postmenopausal women with sexual dysfunction, treated at Menopause Clinic at the Faculty of Medical Sciences of Santa Casa de São Paulo and in the Vale do Sapucai University. All women sign the Consent Form Term. The study will be conducted in accordance with the protocol and principles of the Declaration Helsinki (Version 1996), according to International Conference on Harmonization and Tripartite Guidelines for good clinical practice and regulatory requirements. The protocol was approved by the Ethics Committee of the Faculty of Medical Sciences of Santa Casa de São Paulo.

Hypothesis: It is expected to be an improvement of sexual function in postmenopausal women.

Detailed Description

It will be a prospective, randomized, double-blind, placebo-controlled study with 144 postmenopausal women with sexual dysfunction, met in Menopause Clinic at the Faculty of Medical Sciences of Santa Casa de São Paulo and in the Vale do Sapucai University. All women signed the Informed Consent. The study will be conducted in accordance with the protocol and principles set out in Declaration of Helsinki (1996 version), according to International Conference on Harmonization and Tripartite Guidelines for good practice clinics and applicable regulatory requirements.

The protocol was submitted and approved by the Ethics Committee, Faculty of Medical Sciences Committee Santa Casa de São Paulo. The diagnosis of sexual dysfunction will be done by a sexologist physician experienced and trained in the diagnosis of female sexual disorders through a structured clinical interview, a list of sexual symptoms. It will be oriented to avoid further consumption of diet or another type of herbal medicine during the study. After the interview, signing the Informed Consent and they will be informed about the randomization. Interview with sexological questionnaires will be applied used in Sexology Clinic, Faculty of Medical Sciences of Santa Casa de São Paulo and Vale do Sapucai University, with the purpose of obtaining data sociodemographic. The Female Sexual function Index (FSFI) and the Female Intervention Efficacy Index questionnaire (FIEI). When necessary, the Beck Depression Inventory II (Cunha 2001) will be used to ward off depression, which will be applied by enabled professional. The application will be individually and by the same researcher. The results will be analyzed and interpreted in the light of the theoretical framework of socio-historical psychology, this theory of knowledge, is associated with the understanding of the culture of the structure, social organization and the rescue human subjectivity.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
144
Inclusion Criteria
  • The postmenopausal women with full autonomy, with one year or more of amenorrhea and follicle stimulating hormone (FSH) > 30 milli-International unit/mL
  • Women who are not regularly practicing sexual activity will be included because the desire domain is subject to the same evaluation in this situation
  • Estrogen and progesterone were permitted if the dose had been stable for six months prior to screening
Exclusion Criteria
  • Cardiac, renal and hepatic diseases
  • Diabetes mellitus
  • Cognitive disorders
  • Hormone-dependent tumor
  • History of psychiatric illness current and/or past, regular use of two or more doses of alcohol by day (dose = 12 grams of pure alcohol, which corresponds to 330 mL of beer, 100 mL wine, 30 mL of distilled World Health Organization standard dose) leading to impairment or clinically significant distress (DSM-5)
  • Consumption of Maca supplements or any other nutritional supplement known to cause changes in sexual function
  • Use of any drug that, in the opinion of the investigator, may affect sexual function or any of the following medications: anti-epileptics, cytochrome P450 isoform 3A4 (CYP3A4) inducers
  • Dopamine agonists and other parkinsonian drugs
  • Metoclopramide
  • Androgens and antiandrogens, the anti-oestrogens
  • Fluoxetine or any hormonal implant long-acting in 30 days before the exam
  • Analogues of gonadotropin-releasing hormone and other hormones and inhibitors
  • Benzodiazepines prescribed for insomnia
  • Sedatives and hypnotics
  • Antidepressants
  • Antipsychotics, mood stabilizers, narcotics (except when used to relieve short-term pain),
  • Lubricants/moisturizers that contain substances that promote heating and/or vaginal stimulators

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Placebo GroupThe Female Sexual Function Index (FSFI)The effects of Placebo on sexual function, desire and depression in postmenopausal women. The Female Sexual Function Index (FSFI) and the Female Intervention Efficacy Index Questionnaire (FIEI). The Beck Depression Inventory II will be used to ward off depression
Placebo GroupThe Female Intervention Efficacy Index (FIEI)The effects of Placebo on sexual function, desire and depression in postmenopausal women. The Female Sexual Function Index (FSFI) and the Female Intervention Efficacy Index Questionnaire (FIEI). The Beck Depression Inventory II will be used to ward off depression
Placebo GroupThe Beck Depression Inventory IIThe effects of Placebo on sexual function, desire and depression in postmenopausal women. The Female Sexual Function Index (FSFI) and the Female Intervention Efficacy Index Questionnaire (FIEI). The Beck Depression Inventory II will be used to ward off depression
Placebo GroupPlaceboThe effects of Placebo on sexual function, desire and depression in postmenopausal women. The Female Sexual Function Index (FSFI) and the Female Intervention Efficacy Index Questionnaire (FIEI). The Beck Depression Inventory II will be used to ward off depression
Maca (Lepidium Meyenii Walp) GroupThe Female Sexual Function Index (FSFI)The effects of Lepidium Meyenii Walp on sexual function, desire and depression in postmenopausal women. The Female Sexual Function Index (FSFI) and the Female Intervention Efficacy Index Questionnaire (FIEI). The Beck Depression Inventory II will be used to ward off depression
Maca (Lepidium Meyenii Walp) GroupThe Female Intervention Efficacy Index (FIEI)The effects of Lepidium Meyenii Walp on sexual function, desire and depression in postmenopausal women. The Female Sexual Function Index (FSFI) and the Female Intervention Efficacy Index Questionnaire (FIEI). The Beck Depression Inventory II will be used to ward off depression
Maca (Lepidium Meyenii Walp) GroupThe Beck Depression Inventory IIThe effects of Lepidium Meyenii Walp on sexual function, desire and depression in postmenopausal women. The Female Sexual Function Index (FSFI) and the Female Intervention Efficacy Index Questionnaire (FIEI). The Beck Depression Inventory II will be used to ward off depression
Maca (Lepidium Meyenii Walp) GroupLepidium Meyenii WalpThe effects of Lepidium Meyenii Walp on sexual function, desire and depression in postmenopausal women. The Female Sexual Function Index (FSFI) and the Female Intervention Efficacy Index Questionnaire (FIEI). The Beck Depression Inventory II will be used to ward off depression
Primary Outcome Measures
NameTimeMethod
FSFI Questionnaire to evaluate the sexual function120 days

To study the effects of Lepidium meyenii and placebo on sexual function in postmenopausal women

Secondary Outcome Measures
NameTimeMethod
FIEI Questionnaire to evaluate the sexual desire120 days

To study the effects of Lepidium meyenii and placebo on sexual desire in postmenopausal women

Trial Locations

Locations (1)

Vale Do Sapucai University (Univas)

🇧🇷

Pouso Alegre, MG, Brazil

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