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Compareing effects ofvitexagnus _castus(agnugol) and Placebo on menopausal symptoms

Comparative investigate the effect of vitexagnus _castus(agnugol) and Placebo on menopausal symptoms: a double-blind randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016120528967N3
Enrollment
50
Registered
2016-12-31
Start date
2017-01-08
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 symptoms. Symptoms such as flushing, sleeplessness, headache, lack of concentration, associated with menopause

Interventions

Intervention 1: First group will be given Tab agnugol oral, 2 times daily for 8 weeks. Intervention 2: Second group will be Placebo Tab oral, 2 times daily for 8 weeks.
Treatment - Drugs
First group will be given Tab agnugol oral, 2 times daily for 8 weeks.
Second group will be Placebo Tab oral, 2 times daily for 8 weeks.

Sponsors

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

Eligibility

Sex/Gender
Female
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 65-45 years; at least one year and a maximum of three years of their last menstrual period has passed; the number of hot flashes at least 2 times a day. Exclusion criteria: smoking; at least for a period of 3 months are treated with hormones and antibiotics; systemic diseases such as kidney disease; blood pressure blood sugar; blood fat; depressed and anxious (anxiety and depression diagnosis based on diagnostic criteria DSM5 by psychiatrist); taking antithyroid drugs; gabapentin; SSRI; sulfonamides, methotrexate, Tryamtryn, sulfasalazine; the use of traditional medicines such as drug-induced flushing.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menopausal symptoms. Timepoint: before intervention- 2 weeks later- 4 weeks later- 8 weeks later. Method of measurement: Green Questionnaire.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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