Comparative study of the effectiveness of oral phenytoi
Phase 1
- Conditions
- bipolar.
- Registration Number
- IRCT20101130005280N61
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Patients with bipolar disorder in manic episode based on DSM-5 criteria
Patients should be in the age range of 18 to 40 years
To have the ability to perform and cooperate in psychological tests
Absence of pregnancy and the postpartum period
Not having severe medical illness, especially convulsions
Exclusion Criteria
History of drug sensitivity
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient symptoms(behavioral stability and depression). Timepoint: Before the intervention and 48 hours after the intervention. Method of measurement: Based on daily visits and YMRS, CGI tests.
- Secondary Outcome Measures
Name Time Method