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The effect of Christm in treatment of female sexual disorder

The effect of Crucuma zedoaria (christm) Roscoe capsule in treatment of female sexual disorder in women 18-35 years.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20140525017827N10
Enrollment
74
Registered
2021-07-09
Start date
2021-06-22
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

Female sexual disorder(FSD). Female sexual arousal disorder

Interventions

Intervention 1: Intervention group: 37patient will be received Crucuma zedoaria capsule ( herbal medicine from white turmeric) manufactured by Danesh Bonyan Shafangar Nazari Co. QID for 4 weeks. Inter

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Healthy menstruating women with regular menstrual cycles(between 28-34 days) between 18-35 years of age Being married Documented clinical diagnosis of FSD based on FSFI score. Body mass index (BMI)=LT30. Suffering from FSD for more than 6 months. Nomal sexual function in partner Agree not to use any other form of herbal or hormonal therapies for treatment of sexual dysfunction Women using non hormonal method of contraception to prevent pregnancy.

Exclusion criteria

Exclusion criteria: Pregnancy or attempting to conceive. Breastfeeding within 3 months prior to the study. Having marital discord. Receiving androgen therapy within 3 months of recruitment. Consuming any form of hormonal contraceptive. Consuming drug with a potential to cause sexual dysfunction (such as selective serotonin reuptake inhibitors, tricyclic antidepressants, antihypertensive drugs, etc.) and receiving stations or other drugs known to impact on steroid hormone levels and women who are taking anti-coagulant or anti-platelet drugs in the previous 3 months. Subjects with serious medical conditions such as history of breast, endometrial or other gynecological cancer at any time before study or other cancer within the last 5 years, hypertension, diabetes, tuberculosis, lupus, cardiovascular disease, thrombo-embolic disorders, neurologic or psychiatric disease were also excluded from the study.

Design outcomes

Primary

MeasureTime frame
Female sexual disorder score based on female sexual functin index( FSFI) questionnaire. Timepoint: Before and after the end of the 4-week period of treatment. Method of measurement: female sexual function index( FSFI).;Measurment of testosterone level. Timepoint: Measuring testosterone level before the study and then during the folliculate phase of their next menstural cycle on the day of 7 to 9 after the end of study. Method of measurement: Chemiluminesence Immunoassay (cl).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHoda Nasr Fard Jahromi

Shiraz University of Medical Sciences

hodanasrfard.med@gmail.com+98 71 3648 9830

Outcome results

None listed

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