Health Condition 1: F209- Schizophrenia, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: In-patients satisfying the ICD-11 DCR criteria for schizophrenia. First episode schizophrenia (2years) Age 18-50yrs of both sexes. BMI greater than or equal to 25 kg/m2 CDSS score Those who give written informed consent for participating in the study.
Exclusion criteria
Exclusion criteria: Any other drug(except for Antipsychotics) that can cause weight gain. Patients on 1st generation antipsychotics and or on 1st generation depot antipsychotics. Co-morbid endocrine and/or cardiovascular conditions. Any other major co-morbid psychiatric diagnosis and substance dependence excluding nicotine and caffeine. Known hypersensitivity to Tab. Bupropion or any of its components. Deranged liver function test ( ALT greater than/equal to 180 IU/L and/or AST greater than/equal to 140 IU/L) Significant current/past medical or neurological illness including severe hepatic disease and history of severe head injury. Patients currently receiving ECT. Treatment resistant schizophrenia patients or patients on clozapine. History of suicidality (intent/attempt) QTc interval greater than/equal to 450ms in males and greater than/equal to 470ms in females on Electrocardiogram (ECG). Pregnancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Effectiveness of tab Bupropion XL 300mg/day on metabolic profile in patients of Schizophrenia on second generation anti psychotics assessed by changes in BMI lipid profiles fasting blood glucose & waist circumference and its relationship with BPRS PANSS CGI SCH CDSS SANS MoCA scales.Timepoint: Baseline 4 weeks 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in levels of Melanocyte Stimulating Hormone in patients receiving Tab Bupropion XL 300mg/day.Timepoint: Baseline 4 weeks 8weeks | — |
Countries
India
Contacts
Central Institute of Psychiatry