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Effect of supplementation in treatment of depressio

Phase 3
Conditions
Depression.
Depressive episode
Registration Number
IRCT201412065623N29
Lead Sponsor
Kashan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Patients with major depressive according to DSM-IV-TR criteria
Aged 18 to 65 years
The least score 15 on Hamilton Depression scoring system.

Exclusion Criteria

History of coronary infarction, angina pectoris, stroke or renal stone disease
Pregnant or lactating women
Smokers
Liver problems
Substance abuse
Non-normal creatinine concentrations
Taking dietary supplements during the last 2 months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Depression. Timepoint: At the beginning of the study and after 8 weeks of intervention. Method of measurement: Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Fasting plasma glucose. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic.;Triglycerides. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic.;Total antioxidant capacity. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;Glutathione. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;Cholesterol. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic.;Insulin. Timepoint: Baseline and End-of-trial. Method of measurement: Elisa.
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