Skip to content

The Combined Effect of black cohosh, soybean, arctium lappa L and vitex agnus- castus extracts On menopause

The Combined Effect of black cohosh, soybean, arctium lappa L and vitex agnus- castus extracts on clinical symptoms, biomarkers of oxidative stress biomarkers and inflammation among menopausal women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170430033730N8
Enrollment
54
Registered
2021-03-11
Start date
2021-02-13
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

menopause. Menopausal and other perimenopausal disorders

Interventions

Intervention 1: Intervention group: will receive two capsules of 550 mg of combined extract(Black cohosh, Soybean, Sweet potato, Greater burdock, Vitex) twice daily for 8 weeks. The capsules are ma

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: Having menopausal symptoms

Exclusion criteria

Exclusion criteria: patients who do not want to cooperate People who smoke People who drink alcohol Patients with gastrointestinal disorders Diabetic Patients Thyroid disease, breast and ovarian cancer, liver and neurological disorders, high blood pressure, taking anticoagulants

Design outcomes

Primary

MeasureTime frame
Clinical symptoms. Timepoint: Beginning and end of the study. Method of measurement: Quality of life questionnaire for menopausal women.

Secondary

MeasureTime frame
Glutathione. Timepoint: Beginning and end of the study. Method of measurement: Spectrophotometry.;MDA. Timepoint: Beginning and end of the study. Method of measurement: Spectrophotometry.;TNF-a. Timepoint: Beginning and end of the study. Method of measurement: ELISA.;IL-8. Timepoint: Beginning and end of the study. Method of measurement: ELISA.;Gonadotropins. Timepoint: Beginning and end of the study. Method of measurement: ELISA.;E2. Timepoint: Beginning and end of the study. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Mehdi Mirhashemi

Qazvin University of Medical Sciences

mirhashemism@gmail.com+98 28 3333 6001

Outcome results

None listed

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