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Effect of Of fennel capsule and evening primrose oil on the symptoms of menopause and sex hormones in postmenopausal women

Effect of Of fennel capsule and evening primrose oil on the symptoms of menopause and sex hormones in postmenopausal women who referred to clinics of Shiraz University of Medical Sciences

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160404027207N2
Enrollment
150
Registered
2018-04-24
Start date
2020-05-02
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Menopausal and female climacteric states.

Interventions

Intervention 1: Intervention groups one: The first group of 30 mg capsules of fennel extract for two months and orally twice a day. Intervention 2: Intervention group two: 1000 mg capsules of evening

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Lack of surgery in ovarian tumors Not getting breast cancer treatment (hormone therapy) Failure to receive HRT Women aged 45 to 60 years

Exclusion criteria

Exclusion criteria: Sudden increase or decrease of weight in the sample Any reason that increases or decreases the level of estrogen in the body For any reason, a person has to have hormone therapy Any sign indicating that allergy to fennel and evening primrose oil has manifested itself Examples that can cause menstrual disorder for any reason

Design outcomes

Primary

MeasureTime frame
Menopause symptoms. Timepoint: Before intervention, two months after the intervention. Method of measurement: Hormones, SF36 General Measurement of Quality of Life, MRS A tool for assessing the severity of postmenopausal women's symptoms.

Secondary

MeasureTime frame
Hormonal changes. Timepoint: Before intervention, two months after the intervention. Method of measurement: Elisa Methode.;Evaluation of the quality of life of postmenopausal women. Timepoint: Before intervention, two months after the intervention. Method of measurement: A general tool for assessing the quality of life SF36.;Evaluation of severity of symptoms of postmenopausal women. Timepoint: Before intervention, two months after the intervention. Method of measurement: A special tool for assessing the severity of symptoms of postmenopausal women MRS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGhavi Fatemeh

Shiraz University of Medical Sciences

ghavi.fatemeh@yahoo.com+98 71 3734 0106

Outcome results

None listed

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