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The effect of Valeriana on severity and frequency hot flashes in menopausal women

The clinical trial of valeriana and placebo comparison on severity and frequency of hot flash in menopausal women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201507206888N10
Enrollment
64
Registered
2015-09-11
Start date
2015-12-31
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 flash. Symptoms such as flushing, sleeplessness, headache, lack of concentration, associated with menopause

Interventions

Intervention 1: In intervention group: Sedamin will be prescribed in the form of Oral Capsule 530 mg, Twice in a day along two months. This drug Will be bought from Goldaroo Company in Iran. Intervent
Treatment - Drugs
In intervention group: Sedamin will be prescribed in the form of Oral Capsule 530 mg, Twice in a day along two months. This drug Will be bought from Goldaroo Company in Iran.
In control group: placebo will be prescribed in the form of Oral Capsul contain 530 mg valeriana Twice in a day along two months.

Sponsors

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

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age of between 45-55; elapse of at least one and at most 5 years after menopausal; no using cigarette and alcohol; no having physical or mental diseases; no using of relaxation techniques; no using of hormonal or herbal therapies Exclusion criteria: drug intolerance; not complete treatment duration

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hot flash severity. Timepoint: before the intervention, 1 month after intervention, 2 months after the intervention. Method of measurement: Cooperman Index.;Hot flash frequency. Timepoint: before the intervention, 1 month after intervention, 2 months after the intervention. Method of measurement: Cooperman Index.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Shobeiri

Hamadan University of Medical Sciences

vc_research@umsha.ac.ir+98 81 3838 0150

Outcome results

None listed

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