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Comparing the effect of Fennel extract and placebo on menopausal symptoms

Evaluation the effect of Fennel extract in the treatment of menopausal symptoms compared with placebo

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016120528967N4
Enrollment
50
Registered
2017-02-13
Start date
2017-01-05
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 fennel extract, 2 times daily for 8 weeks. Intervention 2: Second group will be given placebo, 2 time daily for 8 weeks.
Treatment - Drugs
First group will be given fennel extract, 2 times daily for 8 weeks.
Second group will be given placebo, 2 time 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: the women ranging from 45 to 65 years old; menstrual period is elapsed minimally one year and maximally three years; the number of their hot flushes is at least 2 times a day. Exclusion criteria: smoking; undergoing hormone; antibiotics therapy for a period of 3 months at least; systemic diseases such as kidney disease; blood pressure; diabetes; blood fat; depression and anxiety (anxiety and depression diagnosis based on diagnostic criteria DSM5 by psychiatrist); taking anti-thyroid drugs; gabapentin; SSRI; sulfonamides; methotrexate; Tryamtryn; sulfasalazine; estrogen; uptake of traditional medicines such as drug-induced flushing.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Vasomotor. Timepoint: before intervention-2 weeks later- 4 weeks later- 8 weeks later. Method of measurement: Green questionnaire.;Depression. Timepoint: before intervention-2 weeks later- 4 weeks later- 8 weeks later. Method of measurement: Green questionnaire.;Sexual Function. Timepoint: before intervention-2 weeks later- 4 weeks later- 8 weeks later. Method of measurement: Green questionnaire.;Anxiety. 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