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Effect of Foeniculum vulgare seed powder on menopausal symptoms

The effect of Foeniculum vulgare seed powder on estrogen levels, menopausal symptoms and sexual desire in menopausal women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016022125566N4
Enrollment
70
Registered
2016-03-23
Start date
2016-04-03
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

Menopausal. Menopausal and female climactric states

Interventions

Intervention 1: 4 caps of placebo, Every 6 Hours for 8 weeks. Intervention 2: 4 500mg-caps of fennel, Every 6 Hours for 8 weeks.
Placebo
Treatment - Drugs
4 caps of placebo, Every 6 Hours for 8 weeks
4 500mg-caps of fennel, Every 6 Hours for 8 weeks

Sponsors

Vice chancellor for research,Yasuj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Being married and between 40 and 60 years old ; During the past minimum of 12 months and maximum of 5 years have not been menstural periods; With minimum score of 15 in Kupperman Index;Did not recognize diagnosed with mental retardation and hearing and vision problems cognitive; Not received hormone therapy and diet or herbal treatment during the last 6 months ; Lack of chronic diseases (especially epilepsy) Exclusion criteria: Migration;Chronic diseases that have an affected on outcome variables, Consumes less than 80 percent of the drugs in a month

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Estrogen levels. Timepoint: Before the intervention and Two months after the beginning intervention. Method of measurement: According ng / mL by ELISA sensitivity.;Symptoms of menopausal. Timepoint: Before the intervention, Four and eight weeks after the beginning intervention. Method of measurement: Kupperman index.;Sexual desire. Timepoint: Before the intervention, Four and eight weeks after the beginning intervention. Method of measurement: Hullbert Index of Sexual Desire (HISD).

Secondary

MeasureTime frame
Vasomotor symptoms. Timepoint: Before the intervention, Four and eight weeks after the beginning intervention. Method of measurement: Before the intervention, Four and eight weeks after the beginning intervention.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Nazafarin Hosseini

Yasuj University of Medical Science

hosseinichenar@yahoo.com+98 74 3223 4115

Outcome results

None listed

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