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A STUDY TO COMPARE THE WEIGHT, BLOOD SUGAR AND FAT CHANGES IN PATIENTS ON TREATMENT WITH OLANZAPINE, RISPERIDONE AND QUETIAPINE.

â??A CROSS-SECTIONAL STUDY TO COMPARE THE METABOLIC ADVERSE EFFECTS IN PATIENTS RECEIVING TREATMENT WITH OLANZAPINE OR RISPERIDONE OR QUETIAPINE."

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/05/019447
Enrollment
86
Registered
2019-05-30
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: F01-F99- Mental, Behavioral and Neurodevelopmental disorders

Interventions

Intervention1: NIL: NIL

Sponsors

Father Muller Medical College Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients taking antipsychotic treatment with any one of the drugs: Olanzapine, Risperidone, Quetiapine, for a minimum period of 6 months to a maximum period of 1 year.

Exclusion criteria

Exclusion criteria: Not on monotherapy with study drugs Patient is a known case of diabetes or dyslipidemia or has a Pretreatment history of diabetes or dyslipidemia. Patients on Lithium, Nortriptyline, Amitriptyline, valproic acid, antidepressants for past 3 months and other psychotropic agents known to affect insulin sensitivity. Those on other non-psychiatric drugs known to cause weight gain, hyperglycemia or dyslipidemia like steroids, diuretics, hyperglycemia producing antiepileptics. Have current substance abuse or dependency disorder.Pregnancy. Any clinically relevant disease (liver, renal or heart disease).

Design outcomes

Primary

MeasureTime frame
To study the adverse effects on metabolic parameters like weight change from baseline, blood glucose level change and triglyceride level change from normal in patients not previously known to have metabolic abnormalities, receiving treatment with either Olanzapine or Quetiapine or Risperidone.Timepoint: Patients will be assessed at that time point when on treatment with the study drugs for a duration of 6 months to 1 year.

Secondary

MeasureTime frame
To assess the Blood pressure change from baseline in patients receiving treatment with olanzapine or risperidone or quetiapine.Timepoint: Patients will be assessed at that time point when on treatment with the study drugs for a duration of 6 months to 1 year.

Countries

India

Contacts

Public ContactDr Quadros Reshma Ronald

Father Muller Medical College Hospital

padmajaudaykumar@gmail.com9880890512

Outcome results

None listed

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