Skip to content

Tribulus terrestris effect on satisfuction and sexual function

the effect of hydro alcohol extract of teribulus terisris on sexual function and satisfaction in post menopausal women

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016121131340N1
Enrollment
120
Registered
2017-07-23
Start date
2016-12-30
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

sexual dys function. Either the prospect of sexual interaction produces sufficient fear or anxiety that sexual activity is avoided (sexual aversion) or sexual responses occur normally and orgasm is experienced but there is a lack of appropriate pleasure (lack of sexual enjoym

Interventions

Intervention 1: Intervention group 3:The Extract of HydroAlcolol of Teribulus Teristris, Syrup in 0.9 mg/dl Twice per day in 2 months. Intervention 2: Control group: syrups containing mannitol concent
Treatment - Drugs
Intervention group 3:The Extract of HydroAlcolol of Teribulus Teristris, Syrup in 0.9 mg/dl Twice per day in 2 months
Control group: syrups containing mannitol concentration of 0.5 Mg dl, twice a day for two months
Intervention group 1:The Extract of HydroAlcolol of Teribulus Teristris, Syrup in 0.5 mg/dl Twice per day in 2 months
Intervention group 2:The Extract of HydroAlcolol of Teribulus Teristris, Syrup in 0.7 mg/dl Twice per day in 2 months

Sponsors

Ahvaz Jundishapur University of Medical Sciences ,vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion Criteria:Postmenopausal women; reading and writing skills Exclusion Criteria:BMI 30 or higher; use of hormone therapy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sexual Function. Timepoint: Before intervention,After 4 weeks and After 2 months. Method of measurement: FSFI Questionnaire.;Sexual Satisfaction. Timepoint: Before intervention,After 4 weeks and After 2 months. Method of measurement: Larenson Questionnaire.

Secondary

MeasureTime frame
_. Timepoint: _. Method of measurement: _.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMina shojaee

Ahvaz Jundishapur University of Medical Sciences

m.shojaee@ajums.ac.ir+98 61 5335 1538

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026