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The effect of Crocus Sativus in production of happiness and treatment of sextual disorders among menopausal women

The effect of Crocus sativus on happiness and sexual function among menopausal women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015050722099N2
Enrollment
40
Registered
2015-09-11
Start date
2015-08-11
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

Condition 1: sexual function. Condition 2: Happiness. Sexual dysfunction, not caused by organic disorder or disease Other mood [affective] disorders

Interventions

Intervention 1: The interventional group: be taken daily 30 mg oral crocus sativus capsules for 28 days. Intervention 2: The control group: be taken daily 30 mg placebo capsules for 28 days.
Treatment - Drugs
Placebo
The interventional group: be taken daily 30 mg oral crocus sativus capsules for 28 days.
The control group: be taken daily 30 mg placebo capsules for 28 days.

Sponsors

Vice Chancellor for Research of North Khorasan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
49 Years to 34 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Iranian Muslims women;45 to 60 year old women;Fifth grade of Elementray School (in Iran educational sysytem);Married women;Women who passed at least 12 month after the last menstrual period or had more than 40 FSH;Women with natural menopause. Exclusion criteri:Getting the Estrogen/ Progestin Hormone in the last 3 month;spotting in the last year;Using tobacco products (drugs, cigarette, hookah) or alcohol;using of drug/drugs to decrease menopausal symptoms or tranquilizers, antidepressants and anticoagulants in the past month;Having blood pressure more than 160/110;Having stressful life event in the past 6 month;Detecting of a lump or an abnormality in the breast examination or women with malignancecy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Happiness. Timepoint: Before intervention and 4 weeks after taking the capsules. Method of measurement: Oxford Happiness Inventory(OHI).;Sexual Function. Timepoint: Before intervention and 4 weeks after taking the capsules. Method of measurement: Female Sexual Function Index(FSFI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahboobeh Ghorbani

Faculty of Nursing and Midwifery

ghorbani.mahboobeh@gmail.com+98 58 3229 7096

Outcome results

None listed

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