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To Compare the changes in Neurocognitive profile in patients suffering with schizophrenia on treatment with Aripiprazole and Olanzapine

Comparative Efficacy of Aripiprazole and Olanzapine on Neurocognitive Profile of patients with Schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033511
Enrollment
40
Registered
2021-05-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: aripiprazole , olanzapine: Tab. Aripiprazole 10 mg max. upto 30 mg in divided doses daily for 10 weeks. Tab. Olanzapine 5 mg max. upto 20 mg in divided doses daily for 10 weeks. Interve

Sponsors

Government Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: . Patient or nominated representative willing for consent 2. Patient in age group of 18-50years 3. Patients diagnosed with schizophrenia according to DSM 5 criteria with total duration of illness less than 5 years 4. Patients who have never received aripiprazole and/or olanzapine in the past

Exclusion criteria

Exclusion criteria: Patients with Treatment Resistant Schizophrenia (TRS) 2. Patients with neurological disorders â?? head injury, tumours, movement disorders (except antipsychotic induced), dementia, organic brain syndromes (eg. delirium, amnesia), epilepsy. 3. Patients who have received ECT in past 3 months 4. Patients with co-morbid substance dependence (except nicotine and Caffeine) 5. Patients who are lactating or pregnant 6. Patients who received cognitive remediation in recent past. 7. Patients diagnosed with any unstable medical (hypothyroidism, diabetes insipidus, kidney disease, myasthenia gravis, chronic heart disease) or surgical disorders. 8. Patients with subnormal intelligence. 9. Actively Suicidal patients.

Design outcomes

Secondary

MeasureTime frame
scoring on PANSS, BPRS,ASEX,GAS,Timepoint: 0weeks,2weeks,4weeks,6weeks,8weeks and 10 weeks

Primary

MeasureTime frame
comparison between changes in neurocognitive profile on treatment with Aripiprazole and olanzapineTimepoint: Baseline and 10 weeks

Countries

India

Contacts

Public ContactDr Sanya Sharma

Panjab University

ajeetsidana@hotmail.com9646121614

Outcome results

None listed

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