Effects of Lepidium Meyenii Walp on Sexual Function in Postmenopausal Women

NCT ID: NCT02624648

Last Updated: 2016-06-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE1

Total Enrollment

144 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-10-31

Study Completion Date

2016-12-31

Brief Summary

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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

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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.

Conditions

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Sexual Dysfunction, Physiological

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

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Placebo Group

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

Group Type PLACEBO_COMPARATOR

The Female Sexual Function Index (FSFI)

Intervention Type BEHAVIORAL

The Female Sexual Function Index (FSFI) Questionnaire to evaluate the sexual function

The Female Intervention Efficacy Index (FIEI)

Intervention Type BEHAVIORAL

The Female Intervention Efficacy Index Questionnaire (FIEI) to evaluate the sexual function

The Beck Depression Inventory II

Intervention Type BEHAVIORAL

The Beck Depression Inventory II will be used to evaluate or ward off depression

Placebo

Intervention Type DRUG

They will receive a capsule of Placebo twice a day for 120 days

Maca (Lepidium Meyenii Walp) Group

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

Group Type EXPERIMENTAL

The Female Sexual Function Index (FSFI)

Intervention Type BEHAVIORAL

The Female Sexual Function Index (FSFI) Questionnaire to evaluate the sexual function

The Female Intervention Efficacy Index (FIEI)

Intervention Type BEHAVIORAL

The Female Intervention Efficacy Index Questionnaire (FIEI) to evaluate the sexual function

The Beck Depression Inventory II

Intervention Type BEHAVIORAL

The Beck Depression Inventory II will be used to evaluate or ward off depression

Lepidium Meyenii Walp

Intervention Type DRUG

They will receive a capsule of Lepidium Meyenii Walp twice a day for 120 days

Interventions

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The Female Sexual Function Index (FSFI)

The Female Sexual Function Index (FSFI) Questionnaire to evaluate the sexual function

Intervention Type BEHAVIORAL

The Female Intervention Efficacy Index (FIEI)

The Female Intervention Efficacy Index Questionnaire (FIEI) to evaluate the sexual function

Intervention Type BEHAVIORAL

The Beck Depression Inventory II

The Beck Depression Inventory II will be used to evaluate or ward off depression

Intervention Type BEHAVIORAL

Lepidium Meyenii Walp

They will receive a capsule of Lepidium Meyenii Walp twice a day for 120 days

Intervention Type DRUG

Placebo

They will receive a capsule of Placebo twice a day for 120 days

Intervention Type DRUG

Other Intervention Names

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Maca

Eligibility Criteria

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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
Minimum Eligible Age

45 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Irmandade da Santa Casa de Misericordia de Sao Paulo

OTHER

Sponsor Role collaborator

Universidade do Vale do Sapucai

OTHER

Sponsor Role lead

Responsible Party

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Benedito Fabiano dos Reis

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Fabiola SM Campos, MD

Role: STUDY_DIRECTOR

Universidade do Vale do Sapucai

Sonia Maria R Rosa Lima, PhD

Role: PRINCIPAL_INVESTIGATOR

Santa Casa of São Paulo

Locations

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Vale Do Sapucai University (Univas)

Pouso Alegre, Minas Gerais, Brazil

Site Status RECRUITING

Countries

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Brazil

Central Contacts

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BENEDITO FABIANO D REIS, PhD

Role: CONTACT

553534730942

Gustavo Maximiliano D Silva, MD

Role: CONTACT

5511994192039

Facility Contacts

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BENEDITO F REIS, PROF

Role: primary

553599844648

SONIA MARIA R ROSA LIMA, PROF

Role: backup

5511971519229

References

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Chung F, Rubio J, Gonzales C, Gasco M, Gonzales GF. Dose-response effects of Lepidium meyenii (Maca) aqueous extract on testicular function and weight of different organs in adult rats. J Ethnopharmacol. 2005 Apr 8;98(1-2):143-7. doi: 10.1016/j.jep.2005.01.028.

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PMID: 23674952 (View on PubMed)

Gonzales GF, Cordova A, Gonzales C, Chung A, Vega K, Villena A. Lepidium meyenii (Maca) improved semen parameters in adult men. Asian J Androl. 2001 Dec;3(4):301-3.

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PMID: 12472620 (View on PubMed)

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Gonzales GF, Miranda S, Nieto J, Fernandez G, Yucra S, Rubio J, Yi P, Gasco M. Red maca (Lepidium meyenii) reduced prostate size in rats. Reprod Biol Endocrinol. 2005 Jan 20;3:5. doi: 10.1186/1477-7827-3-5.

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Other Identifiers

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CAAE 43373915.3.0000.5479

Identifier Type: -

Identifier Source: org_study_id

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