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Evaluation of the effect of an herbal medication on severity, frequency and duration of hot flashes in menopausal women

The effect of St John's Wort on severity, frequency and duration of hot flashes in peri and postmenopausal women

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT138710241548N1
Enrollment
100
Registered
2009-09-09
Start date
2008-11-09
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

Hot flashes in peri and postmenopausal women. Menopausal and female climacteric states

Interventions

Intervention 1: placebo: 20 drops,three times daily for 2 months. Intervention 2: Hypiran: 20 drops, three times daily for 2 months.
Placebo
Treatment - Drugs
Hypiran: 20 drops, three times daily for 2 months
placebo: 20 drops,three times daily for 2 months

Sponsors

Deputy of Research of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) natural perimenopuse (3-11 months of amenorrhea or increased menstrual irregularity if still cycling) or postmenopause (12 or more months of amenorrhea) (2) untreated complaints for at least 2 months, (3) no history of cancer, (4) moderate to severe hot flashes happening at least once a day, (5) lack of illnesses creating hot flash-like symptoms, (6) presenting the serum level of FSH more than 40 mlu/ml. Exclusion criteria: (1) treatment with sexual hormones, nonhormonal climacteric drugs, or any treatment to alleviate climacteric symptoms in the last 12 weeks before study entry, (2) treatment with chemical or plant-derived medicines in the last 12 weeks before study entry, (3) bilateral oophorectomy, and (4) severe diseases (e.g., of the heart, liver, kidney, alimentary system, or metabolic diseases) or abnormal thyroid-stimulating hormone value that could mimic climacteric complaints or the actual or expected treatment or that could interfere with the study objectives.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Decrease of the severity, frequency and duration of hot flashes. Timepoint: one month. Method of measurement: Kupperman Index.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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