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Effects of Tribulus Terrestris in Women With Hypoactive Sexual Desire Disorder

F

Federal University of Minas Gerais

Status and phase

Completed
Phase 4

Conditions

Hypoactive Sexual Desire Disfunction

Treatments

Other: Placebo
Drug: tribulus terrestris

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Hypoactive Sexual Desire Disorder (HSDD) is the most prevalent female sexual dysfunction in society and is strongly linked to the quality of life of women. The androgen hormones decline over age in the premenopausal period, which occurs around 20 years. 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.

Enrollment

44 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • regular menstrual cycle
  • with no use of hormonal contraception within the last 3 months
  • without any medication, drugs or alcohol.
  • Healthy patients without systemic or psychiatric disease

Exclusion criteria

  • Patients with amenorrhea and/or pregnant.

    • Patients who underwent bilateral oophorectomy.
    • 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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

44 participants in 2 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
patients will use placebo for 120 days
Treatment:
Other: Placebo
Tribulus Terrestris
Experimental group
Description:
patients will use Tribulus terrestris (750 mg/day) during 120 days
Treatment:
Drug: tribulus terrestris

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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