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Comparison of Cariprazine and Risperidone in treatment of Schizophrenia.

Comparative effectiveness and tolerability of Cariprazine and Risperidone in persons with Schizophrenia. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057293
Enrollment
70
Registered
2023-09-06
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: F20- Schizophrenia

Interventions

Intervention1: Cariprazine: Antipsychotic drug Dose: 1.5-6 mg Frequency: daily Route: oral Duration: 10 weeks Control Intervention1: Risperidone: Antipsychotic drug Dose: 2-16 mg Frequency: daily Rout

Sponsors

Government Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Persons diagnosed with Schizophrenia as per ICD-11. 2. Persons of all genders, aged between 18-65 years. 3. Drug naïve patients only. 4. Duration of illness not more than 2 years. 5. Patients or Nominated representatives (in case of patients who lack capacity for making decisions for treatment as per Mental Healthcare Act-2017) willing to give consent for the study. 6. Patients being accompanied by reliable informants.

Exclusion criteria

Exclusion criteria: 1. Patients with neurological disorders - head injury, tumours, dementia, organic brain syndromes (e.g. delirium, amnesia), epilepsy. 2. Patients with co-morbid substance dependence (except Nicotine and Caffeine). 3. Patients who are lactating or pregnant. 4. Patients with Intellectual disability. 5. Actively suicidal patients. 6. Patients with any acute, unstable medical/surgical illnesses.

Design outcomes

Primary

MeasureTime frame
Change in the severity of psychiatric symptomatology as measured by PANSS, BPRS.Timepoint: 0, 2, 4, 7, 10 weeks

Secondary

MeasureTime frame
Effect of treatment on quality of life, current functioning & neuropsychological assessments as measured on CDSS, WHOQOL BREF, GASS, SOFS, CGI, ASEX, MOCA, blood & other related investigations.Timepoint: 0, 2, 4, 7, 10 weeks

Countries

India

Contacts

Public ContactDr Ajeet Sidana

Government Medical College and Hospital, Sector 32, Chandigarh

ajeetsidana@hotmail.com9056422679

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026