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Effects of Licorice on Relief and Recurrence of Menopausal Hot Flashes

Effects of Licorice on Relief and Recurrence of Menopausal Hot Flashes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103264317N3
Enrollment
90
Registered
2011-05-15
Start date
2009-03-20
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. Menopausal and female climacteric states

Interventions

Intervention 1: Licorice capsules contained 330mg licorice root abstract.The subjects took them for 8 weeks 3 times a day (morning, noon and night). Intervention 2: Placebo capsules had 330mg starch
Treatment - Drugs
Placebo
Licorice capsules contained 330mg licorice root abstract.The subjects took them for 8 weeks 3 times a day (morning, noon and night).
Placebo capsules had 330mg starch with the same shape. The subjects in control group took them for 8 weeks 3 times a day (morning, noon and night).

Sponsors

Sbmu Pharmaceutical Sciences Research Center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: The subjects were between 45-60, had body mass index (BMI) under 29, experienced amenorrhea at least 1 year or at most 3 years, suffered from hot flash and used no drug or hormone to relieve it. In addition, they had no known disease in their medical records, didn’t take antidepressants or sedatives, were married or lost their husbands not sooner than 1 year, experienced no stressful event (e.g. death of close family members, divorce etc.) in the past 6 months, were not vegetarian or had no allergy to herbs as well as no history of estrogenic cancers in themselves or their close relatives. Exclusion criteria: The subjects were decided to use drug or hormone and herbals medicin to relieve hot flashes.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of hot flash. Timepoint: At the end of each week, for 2 weeks before the intervention , for 8 weeks of the intervention for 4 weeks of followed up stage. Method of measurement: Information form.;Relief. Timepoint: Weekly. Method of measurement: Information form.;Recurrence. Timepoint: Weekly. Method of measurement: Information form.;Frequency of hot flash. Timepoint: At the end of each week, for 2 weeks before the intervention , for 8 weeks of the intervention for 4 weeks of followed up stage. Method of measurement: Information form.

Secondary

MeasureTime frame
Daily food intake. Timepoint: At the end of each week. Method of measurement: Information form.;Blood pressure. Timepoint: Weekly. Method of measurement: Sphygmomanometer( instrument for measuring blood pressure).;Weight. Timepoint: Weekly. Method of measurement: Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Nahidi

Shaheed Beheshti University of Medical Sciences and Health Services

nahidifateme@yahoo.com+98 21 2243 9912

Outcome results

None listed

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