Validation of concomitant medications affecting lamotrigine blood levels
Phase 1
Recruiting
- Conditions
- Bipolar disorder, epilepsy
- Registration Number
- JPRN-jRCT1061220093
- Lead Sponsor
- Ishizawa Keisuke
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
1. cases in which LTG was prescribed for the treatment of psychiatric disorders in our psychiatry department
2. cases in which the patient (or a substitute) has given written consent
Exclusion Criteria
1. patients under 18 years of age
2. patients for whom it is impossible to measure LTG blood concentration due to the unavailability of samples necessary for the measurement
3. patients whose consent could not be obtained
4. other patients deemed ineligible by the physician in charge
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method