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Effects of Tribulus Terrestris in Postmenopausal Women With Hypoactive Sexual Desire Disorder

Effects of Tribulus Terrestris in Postmenopausal Women With Hypoactive Sexual Desire Disorder

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01975649
Enrollment
44
Registered
2013-11-05
Start date
2013-06-30
Completion date
2015-04-30
Last updated
2015-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Menopause, Sexual Abstinence

Keywords

postmenopausal, hypoactive, sexual disorder, androgen

Brief summary

Hypoactive Sexual Desire Disorder ( HSDD ) is very common in postmenopausal women due to a reduction in circulating androgen levels. The aim of this study is to evaluate the effects of Tribulus Terrestris in premenopausal women with HSDD.

Detailed description

Hypoactive Sexual Desire Disorder ( HSDD ) is the most prevalent female sexual dysfunction in society mainly in postmenopausal women, and is strongly linked to the quality of life of women . The androgen hormones decline over age in the premenopausal period, more sharply after menopause. Tribulus terrestris is a plant native to India , recommended in the treatment of infertility , low libido and impotence . Its main active ingredient is the protodioscin , which has been attributed to an increase in testosterone levels and improved sexual function . The aim of this study is to evaluate the effects of Tribulus Terrestris in premenopausal women with HSDD .

Interventions

patients will use 750 mg/day during 120 days

OTHERPlacebo

patients will use placebo pills with the same shape of the drug

Sponsors

Federal University of Minas Gerais
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
50 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* at least one year after last menstrual period * with no use of hormonal replacement therapy within the last 3 months * without any medication, drugs or alcohol. * Healthy patients without systemic or psychiatric disease

Exclusion criteria

* Patient smoker (10 cigarettes per day). * Patients with blood pressure \> 160/90 mm Hg. * Patient with breast or endometrial carcinoma. * Patients with a history of myocardial infarction. * Patient with Diabetes. * Patient with vaginal bleeding from any source. * Patients with hepatic injury. * Patients with active thrombophlebitis or thromboembolic disorders recent * Patients with interpersonal relationship problems with your relationship or partner * Patients with sexual problems from your partner

Design outcomes

Primary

MeasureTime frameDescription
Sexual Desire120 dayswe will use the Quotient Sexual - Version Feminine (QS-F) brazilian questionary to make the evaluation

Secondary

MeasureTime frameDescription
serum levels of prolactin and thyroid-stimulating hormone (TSH)120 daysBlood test

Other

MeasureTime frameDescription
serum levels of testosterone and sex hormone-binding globulin (SHBG)120 daysBlood test

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026