Topiramate vs Metformin on Cardio-Metabolic Profile in Schizophrenia on Atypical Antipsychotics

NCT ID: NCT05663749

Last Updated: 2023-08-22

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-09-20
• Study Completion Date: 2023-08-20

Brief Summary

Metabolic syndrome is common in patients of schizophrenia. It can add to morbidity, loss of functionality and discontinuation of antipsychotic medication. Apart from metformin, there are limited treatment options as add on-s to antipsychotics for treatment of metabolic syndrome. There have been placebo-controlled studies of Topiramate as an adjuvant but the present study would be the first head-on trial between these drugs for treatment of metabolic syndrome in patients of schizophrenia.

If the outcome measures show a significant improvement with add on topiramate when compared with Metformin, then add on Topiramate can be a preferred treatment for metabolic syndrome in patients with schizophrenia on atypical antipsychotics. The adverse effects of Metformin can be side-stepped and Topiramate can also be given in conditions which are contraindications for Metformin. Thus, Topiramate can be a good alternative to metformin especially in conditions like liver, cardiac and renal impairment where metformin use should be avoided. Topiramate can not only improve metabolic parameters but can also have a beneficial effect on the symptom severity of schizophrenia. Thus, it can be a good augmentation drug to be used along with antipsychotics in these patients.

Detailed Description

Study Design: The proposed study will be a randomised, parallel arm, active controlled, open label, clinical trial.

Study Setting: The proposed study will be conducted at the out-patient (OP) and the in-patient (IP) settings of the Department of Psychiatry, All India Institute of Medical Sciences, Bhubaneswar.

Study Groups: The study population will comprise of 60 patients with schizophrenia (F20 according to ICD 10 DCR) on atypical antipsychotics for more than 3 months diagnosed with metabolic syndrome.

Sample size: Sample size calculation has been done based on the expected difference in the cardiovascular risk scoring (QRISK3), the primary outcome measure of our study. Sample size of 23 per group will achieve a power of 80%, to detect the difference of 5% in cardiovascular risk scoring (QRISK3) between the groups with standard deviation as 6.0 and a level of significance 0.05. Assuming an attrition rate of 25%, 30 patients will be recruited per group.

Details of Control(s): It is an active controlled study where the control group will receive add-on metformin along with the ongoing atypical antipsychotic.

Details of intervention:

The patients who are randomized to Topiramate group will be receiving Topiramate at a stable dose of 50 mg/day during the study period that is for 8 weeks along with the ongoing atypical antipsychotic.

The patients who are randomized to Metformin group will be receiving Metformin at dose of 500 mg/day twice a day, a total of 1000 mg/day for 8 weeks along with the ongoing atypical antipsychotic.

Duration of study: The study will be conducted for a period of 18 months

Investigation specifically related to Protocols:

The following Psychiatric scales will be used:

1. PANSS: The Positive and Negative Syndrome Scale

2. CGI-SCH Scales: The Clinical Global Impression-Schizophrenia scale (for Severity and Improvement) The following investigations will be done for cardio-metabolic profile;

a) QRISK3 b) Lipid profile c)Fasting serum insulin by ELISA for insulin resistance (HOMA-IR) d)Fasting blood glucose for insulin resistance (HOMA-IR)

Conditions

Metabolic Syndrome; Schizophrenia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Metformin arm

1000mg for 8 weeks

Group Type: ACTIVE_COMPARATOR

Metformin

Intervention Type: DRUG

1000mg for 8 weeks

Topiramate arm

50mg for 8 weeks

Group Type: EXPERIMENTAL

Topiramate

Intervention Type: DRUG

50mg for 8 weeks

Interventions

Metformin

1000mg for 8 weeks

Intervention Type: DRUG

Topiramate

50mg for 8 weeks

Intervention Type: DRUG

Other Intervention Names

Dibeta SR; Metgen; Glycomet; Topamax; Topirol; Topaz

Eligibility Criteria

Inclusion Criteria

• Patients clinically diagnosed with schizophrenia (F20 according to ICD-10 DCR) on a stable dose of atypical antipsychotic for more than 3 months.
• Patients with metabolic syndrome (as per NCEP ATP III Definition).
• Patients above 25 years of age of either gender.
• Legally authorized representative (LAR) giving voluntary written consent for participation in the study.

Exclusion Criteria

• Patients on combination of antipsychotics.
• Patients having any contraindication for Metformin/Topiramate.
• History of any psychoactive substance use in harmful use or dependence pattern except tobacco.
• Any co-morbid medical, psychiatric or neurological disorders like hypertension, coronary artery disease, hypothyroidism, arthritis.
• History of any significant head injury or organic diseases.
• Pregnant and breastfeeding females.

• Minimum Eligible Age: 25 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

All India Institute of Medical Sciences, Bhubaneswar

OTHER

Sponsor Role: lead

Responsible Party

BISWA RANJAN MISHRA

Additional Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Biswa Ranjan Mishra, MD, DPM

Role: PRINCIPAL_INVESTIGATOR

All India Institute of Medical Sciences, Bhubaneswar

Locations

Dept of Psychiatry, Aiims, Bhubaneswar

Bhubaneswar, Odisha, India

Countries

India

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Other Identifiers

AIIMS BBSR/PG Thesis/2021-22

Identifier Type: -

Identifier Source: org_study_id