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effect of a combinatory medication on the basis of black seed on the sexual function of women.

Topical effect an oil, derived from black seed, on women's sexual function: A pilot clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190527043729N1
Enrollment
40
Registered
2019-07-28
Start date
2019-03-11
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Condition 1: Sexual dysfunction. Condition 2: Lack or loss of sexual desire. Condition 3: Lack or loss of sexual enjoyment. Condition 4: Lack or loss of female sexual arousal disorder. Sexual dysfunction not due to a substance or known physiological condition Hypoactive sexual desire disorder Sexual aversion disorder Female sexual arousal disorder

Interventions

Intervention group: The study consists of one group and the intervention is the same for all. 40 women with an age range of 18- 35 years with sexual dysfunction are selected for the study, according t

Sponsors

Karaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Married women with a stable life with their spouse having the least reading and writing education skills. having intercourse of three times or more during the study.

Exclusion criteria

Exclusion criteria: Diagnosis of chronic physical, psychological and behavioral illnesses. being multi-partner using hormonal drugs and drugs affecting sexual function. pregnancy, lactation, and menopause.

Design outcomes

Primary

MeasureTime frame
Score of sexual function based on Female sexual function index questionnaire. Timepoint: Measurement of sexual function at the time of entering the study (before intervention), on the seventh day, and on the 14th day, After starting the oil based on black seed. Method of measurement: Female sexual function index questionnaire.;Score of sexual desire or interest based on Female sexual function index questionnaire. Timepoint: Measurement of sexual function at the time of entering the study (before intervention), on the seventh day, and on the 14th day, After starting the oil based on black seed. Method of measurement: Female sexual function index questionnaire.;Score of satisfied in sexual relationship based on Female sexual function index questionnaire. Timepoint: Measurement of sexual function at the time of entering the study (before intervention), on the seventh day, and on the 14th day, After starting the oil based on black seed. Method of measurement: Female sexual function index questionnaire.;Score of sexual arousal based on Female sexual function index questionnaire. Timepoint: Measurement of sexual function at the time of entering the study (before intervention), on the seventh day, and on the 14th day, After starting the oil based on black seed. Method of measurement: Female sexual function index questionnaire.;Score of maintain vaginal lubrication until completion of intercourse based on Female sexual function index questionnaire. Timepoint: Measurement of sexual function at the time of entering the study (before intervention), on the seventh day, and on the 14th day, After starting the oil based on black seed. Method of measurement: Female sexual function index questionnaire.

Secondary

MeasureTime frame
Skin itching. Timepoint: On the seventh day, and on the 14th day, After starting the oil based on black seed. Method of measurement: Observation.;Skin irritation. Timepoint: On the seventh day, and on the 14th day, After starting the oil based on black seed. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Ghanbaryan

Tehran University of Medical Sciences

lghanbaryan@yahoo.com+98 61 5283 2978

Outcome results

None listed

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