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Lipid changes in schizophrenia patients compared to healthy controls

Lipidomic changes in drug-naïve/drug-free schizophrenia patients compared to healthy controls and its association with clinical outcome: An observational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/08/035496
Enrollment
108
Registered
2021-08-06
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: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Shivaprakash G
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Cases: Objective 1 1. All diagnosed schizophrenia cases who are antipsychotic drug-free defined as 1 month for oral drugs and 3 months for injectable depots at the time of recruitment. 2. Drug-naïve schizophrenia cases diagnosed as per DSM- 5 by the psychiatrist, presenting at psychiatry department will be included. Control: The healthy control group, matched for age, gender [among the hospital staff and their family members and friends of same community with no personal and family history [I and II degree relatives] of psychotic illness. Objective 2 &3 : Inclusion All drug-naïve and drug-free SCZ patients diagnosed as per DSM 5 who were started with antipsychotic drugs

Exclusion criteria

Exclusion criteria: Objective 1 •Metabolic syndrome and other medical disorders, acutely ill cases, cancer •Patient on history of taking antipsychotics within last 1 month for oral drugs and 3 months for depot formulation, cholesterol lowering agents, substance abuse, immunomodulatory treatment •Dietary supplementation with Polyunsaturated fatty acids or other lipids as therapy. Objective 2 and 3: •Metabolic syndrome and other medical disorders, acutely ill cases, cancer •Patient on cholesterol lowering agents, substance abuse, immunomodulatory treatment •Dietary supplementation with Polyunsaturated fatty acids or other lipids as therapy

Design outcomes

Primary

MeasureTime frame
Blood for Lipidomics of Extracellular Vesicles in both cases and control groups at V0 and V2; BPRS, Cognition assessments in cases at V2Timepoint: Baseline V0 and V2 at 8±2 weeks

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactShivaprakash G

KMC, Manipal

smita.shenoy@manipal.edu0820-2922083

Outcome results

None listed

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