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The effect of Salvia officinalis on lipid profile and quality of life in postmenopausal wome

Phase 2
Completed
Conditions
Menopausal and femal climacteric state.
Menopausal and other perimenopausal disorders
N95.1
Registration Number
IRCT20140622018187N12
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
102
Inclusion Criteria

Age between 45 and 60 years
Menstruation in the past year
Conscious written consent
No known physical or mental illness
Do not take any hormonal medications to reduce menopausal symptoms in the past month
Do not take lipid-lowering drugs
BMI below 29
No history of allergy to herbal medicines
No smoking, hookah or drug addiction

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cholesterol. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Laboratory.;Triglycerides. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Laboratory.;HDL. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Laboratory.;LDL. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Laboratory.
Secondary Outcome Measures
NameTimeMethod
Menopause Quality Of Life. Timepoint: 1 week before the intervention and 8 weeks after intervention. Method of measurement: Menopause Quality Of Life Questionnaire.
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