Skip to content

Effects of oral ginger capsules on sexual function women

Effects of oral ginger capsules on sexual function and sexual quality of life of married women in the reproductive age

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191013045086N1
Enrollment
190
Registered
2019-12-22
Start date
2019-07-21
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

Sexual dysfunction. Sexual dysfunction not due to a substance or known physiological condition

Interventions

Intervention 1: Intervention group: 95 women who were included in the study according to inclusion criteria. They will consume 4 tablets of 250 mg oral ginger daily prepared by Isfahan Flower Drug Com

Sponsors

The University of Trabiat Modares
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: Reproductive aged women (age: 18-49 years old) Having sex at least twice a month Lack of known underlying disease Lack of mental illness Being a single spouse and living with the spouse now and during the study Can read and write the Persian language Being Iranian Couples not being addicted to drugs or alcohol No-use of drugs that affect the function of the genus No stressful accident during the past month No urinary tract infection Absence of active or lesion in genital area that interferes with sexual intercourse No history of infertility No record of pelvic surgeries No allergy to ginger Absence of pregnancy or lactation

Exclusion criteria

Exclusion criteria: Unwilling to stay in study Not taking ginger capsules Ginger allergy or complications during the intervention Creating active or lesion in the genital area that interferes with intercourse during intercourse Use of drugs that affect sexual function during the intervention Experiencing a stressful accident during the intervention Urinary tract Infection during Intervention

Design outcomes

Primary

MeasureTime frame
Scores obtained from the Female Sexual Function scale. Timepoint: Assessment of sexual function before and 4 weeks after intervention. Method of measurement: Female sexual function scale.;Scores obtained from the Sexual Quality of Life-Female (SQOL-F) questionnaire. Timepoint: Assessment of sexual quality of life before and 4 weeks after intervention. Method of measurement: Sexual Quality of Life-Female (SQOL-F) questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShadab Shahali

Tarbiat Modares University

shadab.shahali@modares.ac.ir+98 21 8288 3811

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 12, 2026