Topiramate’s effectiveness on weight reduction and metabolic syndrome in obese patients with schizophrenia and schizoaffective
Phase 3
- Conditions
- Schizophrenia,Schizoaffective.
- Registration Number
- IRCT20210622051665N1
- Lead Sponsor
- niversity of social welfare and rehabilitation sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Age between 18 to 65 years
BMI above 27
Patients with schizophrenia or schizoaffective disorder receiving a second-generation antipsychotic drug
Obtaining informed consent from the patient and the patient's legal guardian
Exclusion Criteria
Diabetis
Pregnancy or breastfeeding
Patients with heart failure
Patients with kidney disease
Hypersensitivity to topiramate
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method BMI>27. Timepoint: before study and in weeks 4,8 and 12. Method of measurement: measure height and weight.;Measure abdominal circumference. Timepoint: before study and in weeks 4,8 and 12. Method of measurement: Tape meter.;FBS. Timepoint: before the study and in weeks 4,8 and 12. Method of measurement: Blood sample and lab result.;Total cholesterol. Timepoint: before the study and in weeks 4,8 and 12. Method of measurement: Blood sample and lab result.;Triglyceride. Timepoint: before the study and in weeks 4,8 and 12. Method of measurement: Blood sample and lab result.
- Secondary Outcome Measures
Name Time Method