Effect of Melissa Officinalis and lavandula angustifolia in treatment of depressio
Not Applicable
- Conditions
- Major depressive disorder.Depressive episode
- Registration Number
- IRCT2014061718126N1
- Lead Sponsor
- Shahed University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
age 18 - 65 years old; DSM-V criteria for major depressive disorder(mild to moderate); signed informed consent.
Exclusion criteria: positive history of other psychological disorders; consumption of alcohol or other addictive substances in last 2 weeks; serious medical disease; allergic reaction to medical herbs; positive history of suicidal attempt or suicidal intention; pregnancy; consumption of thyroid disorders drugs.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of depression. Timepoint: Baseline,2 , 4 and 8 weeks after starting the medication. Method of measurement: Hamilton rating scale for depression.
- Secondary Outcome Measures
Name Time Method Side Effects. Timepoint: 0-2-4-8 weeks. Method of measurement: Clinical interview and physical examination and checklist.