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A TRIAL TO STUDY THE EFFECTS OF ATORVASTATIN IN PATIENTS WITH CHRONIC SCHIZOPHRENIA

ATORVASTATIN AS AN ADJUNCTIVE THERAPY IN PATIENTS OF SCHIZOPHRENIA AND ITS RELATION TO C REACTIVE PROTEIN:A RANDOMISED PLACEBO CONTROLLED OPEN LABEL STUDY

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/017304
Enrollment
60
Registered
2019-01-31
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: Atorvastatin: 40 mg oral tablet daily for 6 weeks Control Intervention1: Placebo of tablet Atorvastatin: 40 mg daily oral tablet for 6 weeks

Sponsors

CENTRAL INSTITUTE OF PSYCHIATRY
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a) Patients admitted in the Institute and satisfying the ICD 10-DCR[1993] criteria for schizophrenia[ with illness duration more than or equal to 2 years] b) Age group of 18-50 years of both sexes c) Drug naive patients or drug free for minimum 2 weeks on oral antipsychotics & 4 weeks for depot preparation d) Those who give informed consent for participating in the study.

Exclusion criteria

Exclusion criteria: a) Any other major co-morbid psychiatric diagnosis and substance dependence excluding nicotine & caffeine. b) Significant medical or neurological illness including severe cardiovascular, hepatic, renal,[serum creatinine > 1.5 mg/dl], anaemia [Haemoglobin 8 | P a g e d) BMI >30 kg/m2 e) Not willing to give written informed consent f) Current treatment with Insulin, medications known to affect glucose tolerance anti-inflammatory drugs including NSAIDS, thiazide diuretics, agents that induce weight loss]. g) Current treatment with drugs that induce or inhibit metabolism of statins [Azole antifungals, Macrolide antibiotics, Carbamazepine, anti-retroviral protease inhibitors] h) Known hypersensitivity to Tab. Atorvastatin or any of its components i) Any current systemic infection/ inflammation

Design outcomes

Primary

MeasureTime frame
Improvement in positive,negative,cognitive symptomsof Schizophrenia and decrease in the level of C Reactive ProteinTimepoint: 2 weeks,6 weeks

Secondary

MeasureTime frame
Change in the metabolic profile of the patientsTimepoint: 2 weeks, 6 weeks

Countries

India

Contacts

Public ContactDebasmita Dey

CENTRAL INSTITUTE OF PSYCHIATRY

dram_cip@rediffmail.com6512450448

Outcome results

None listed

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