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The effect of gensing on sexual function in postmenopausal women with major depressio

Phase 2
Recruiting
Conditions
Major depression.
Depressive episode
Registration Number
IRCT20120718010324N74
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
66
Inclusion Criteria

Postmenopausal women with major depressive disorder confirmed by the psychiatrist colleague of the research team
Age 40-65 years
Having a steady sexual partner
Having sexual intercourse at least once a month
At least 12 months have passed since their last period.
FSFI score less than 28
No change in treatment plan during the past and future 2 months (including no current treatment, stable use of antidepressants, or continuous non-pharmacological treatment)
Having reading and writing literacy

Exclusion Criteria

Having chronic diseases, including cardiovascular, liver, diabetes, kidney and endocrine diseases, according to medical records
Hormone therapy for any reason during the last 2 months
Blood pressure above 140/90 based on measurement by the researcher and medical records
Continuous use of other herbal medicines
Taking medications that interfere with ginseng, such as diabetes medications, immunosuppressants, and warfarin
Having a history of allergy to herbal medicines

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sexual function. Timepoint: Before and after the end of intervention. Method of measurement: Female Sexual Function Index.
Secondary Outcome Measures
NameTimeMethod
Menopausal symptoms. Timepoint: Before and after the end of intervention. Method of measurement: Green scale.;Depression. Timepoint: Before and after the end of intervention. Method of measurement: Beck depression questionnaire.;Side events. Timepoint: During the intervention. Method of measurement: Side events checklist.
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