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Evaluation of the effect of Modafinil in the treatment of major depressive disorder

Phase 3
Conditions
Major depressive disorder.
Major depressive disorder, single episode
Registration Number
IRCT20180522039784N1
Lead Sponsor
Karaj University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Diagnosis of major depressive disorder
Informed consent

Exclusion Criteria

Diagnosis of bipolar mood disorder, ADHD or any underlying medical disease
Use of any illicit drugs
Use of any medication that interferes modafinil action
Past history of suicide
Past history of receiving ECT
Pregnancy
Daily use of more than 250 mg of caffeine

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fatigue severity. Timepoint: Before intervention and 6 weeks after initiation. Method of measurement: Fatigue severity scale.;Mood cahnges. Timepoint: Before intervention and 6 weeks after initiation. Method of measurement: Beck's depression inventory.
Secondary Outcome Measures
NameTimeMethod
Drug side effects. Timepoint: Six weeks after intervention. Method of measurement: Obtaining history.
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