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A clinical trial to study effects of oral and long acting injectable antipsychotic in patients with schizophrenia.

Comparative efficacy, tolerability and treatment adherence of oral and long acting injectable antipsychotic in first episode schizophrenia.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/02/023446
Enrollment
60
Registered
2020-02-19
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: Oral Haloperidol: First generation antipsychotic, Dose will be given as per the treating consultant based on efficacy and tolerability and the effects will be monitored at week 2, 4, 6,

Sponsors

Government Medical College and Hospital Chandigarh Sector
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients diagnosed with schizophrenia as per DSM-5 2) Total duration of illness shall be less than one year. 3) Age of the patients shall be between 18-45 years. 4) Drug naïve or not on any psycho tropics for 2 weeks. 5) Patients willing to participate and give consent or in case the patient lacks mental capacity, his/her nominated representative gives consent to participate.

Exclusion criteria

Exclusion criteria: 1) Patients who are not willing to give consent. 2) Pregnant and breast feeding patients. 3) Patients with co-morbid psychiatric illness and substance dependence. 4) Patients with severe medical and surgical illness. 5) Patients with high suicidal risk( Beckâ??s scale for suicidal ideation score >29) 6) Patients with history of sensitivity to haloperidol in the past. 7) Patients with history of depot antipsychotic administration in the past. 8) Patients with no response to haloperidol in the past or those reporting non-tolerability to the drug in the past. 9) Patients who had received ECT in the past.

Design outcomes

Primary

MeasureTime frame
To compare the efficacy and safety profile of oral and long acting injectable haloperidol in patients with first episode schizophrenia.Timepoint: Baseline, week 2, week 4, week 6, week 8, week 12

Secondary

MeasureTime frame
To compare quality of life in patients with first episode schizophrenia on oral and long acting injectable haloperidol. Timepoint: Baseline, week 4, week8, week 12

Countries

India

Contacts

Public ContactRamandeep Kaur

Government Medical College and Hospital, Chandigarh

malhotra.nidhi05@gmail.com9417457554

Outcome results

None listed

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