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Allopurinol as an Adjunctive Therapy in Patients with Bipolar Mania

Allopurinol as an Adjunctive Therapy in Patients with Bipolar Mania as Monitored by Serum Uric Acid Level - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058864
Enrollment
90
Registered
2023-10-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: F312- Bipolar disorder, current episodemanic severe with psychotic features

Interventions

Intervention1: Allopurinol: Tablet Allopurinol 300 milligrams twice daily given orally for 4 weeks in Patients Of Bipolar Mania Along with a Single Mood stabilizer and An Antipsychotic. Control Interv

Sponsors

Central Institute Of Psychiatry
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male inpatients satisfying the ICD 10-DCR[1993] criteria of Bipolar affective disorder, current episode mania with psychotic symptoms with YMRS score of >20 and HAMD score 2. Age group of 18-50 years. 3. Drug naive or drug free patients for minimum 2 weeks for mood stabilizers/antipsychotics and 4 weeks for depot antipsychotics. 4. Those who give informed consent for participating in the study.

Exclusion criteria

Exclusion criteria: 1. Any other major co-morbid psychiatric diagnosis and substance dependence excluding nicotine & caffeine. 2. Significant current/ past medical or neurological illness including severe hepatic disease and history of severe head injury. 3. Patients taking antipurinergic drugs for other medical conditions. 4. Known hypersensitivity to Tab. Allopurinol or any of its components. 5. Patients who had received ECT in last 6 months.

Design outcomes

Primary

MeasureTime frame
Effectiveness Of Allopurinol (600MG/Day)as an Adjunctive Therapy as Assessed ON YMRS, BPRS, and ,OAS-M ,HAMDTimepoint: Baseline And 4 Weeks

Secondary

MeasureTime frame
CHANGE IN SERUM URIC ACID LEVEL IN PATIENTS RECEIVING TAB ALLOPURINOL 600MG/DAYTimepoint: BASELINE AND 4 WEEKS

Countries

India

Contacts

Public ContactDr Alok Pratap

CENTRAL INSTITUTE OF PSYCHIATRY

DRALOKPRATAP@gmail.com7781803812

Outcome results

None listed

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