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Comparison of the effect of Agnugol, Cimifugol , Soyagol , vitagnus and EsCitalopram

Phase 3
Recruiting
Conditions
Menopause.
Menopausal and female climacteric states
N95.1
Registration Number
IRCT20080902001181N4
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
200
Inclusion Criteria

Obtaining a score of 5 and above from the MRS questionnaire
12 months or more have passed since menopause
Age between 45 and 65 years

Exclusion Criteria

Presence or history of breast and uterine cancer, abnormal vaginal bleeding, liver, kidney, thyroid, depression and known anxiety disorders.
Use of progestins, contraceptive pills, GNRH agonists and antagonists
Taking drugs that interact with the studied drugs, such as warfarin, tamoxifen, antipsychotics, and dopamine antagonists.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total score of menopausal symptoms. Timepoint: The total score of menopausal symptoms is checked at the beginning of the study (before the start of the intervention), the fourth and the eighth week after the start of the intervention. Method of measurement: Menopause Rating Scale (MRS).
Secondary Outcome Measures
NameTimeMethod
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