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The effect of Salvia officinalis on hot flush and night sweat in menopausal women

Effect of Salvia officinalis Tablet on hot flash, night sweating and estradiol hormone in postmenopausal women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014062218187N1
Enrollment
100
Registered
2014-07-22
Start date
2014-05-22
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 and femal climacteric state. Menopausal and other perimenopausal disorders

Interventions

Treatment - Drugs
Salvia officinalis extract, 100 mg tablet, three times daily for 8 weeks.
Placebo, tablets 100 mg, three times daily, 8 weeks.

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Women between 45 to 60 years old who are less than 5 years after menopause; At least 12 months since last menstruation; At least three hot flushes daily; Written informed consent; No known physical or mental illness; Not using any medication with influence on menopausal symptoms within three month before the study start; BMI less than 29; No history of allergy to herbal medicine; No smoking or addiction; No use of medication with influence on menopausal symptoms. Exclusion criteria:Use of medication with influence on menopausal symptoms; Allergy to the medicine used or not used in the study; Patient reluctance

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hot flash. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Questionnaire.;Night sweats. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Questionnaire.;Estradiol. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Laboratory pg per ml.

Secondary

MeasureTime frame
Menopausal Symptoms. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Menopause Rating Scale questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSedighe Forouhari

Shiraz University of Medical Sciences

forouharism@yahoo.com+98 71 1647 4257

Outcome results

None listed

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