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

Primary Purpose

Metabolic Syndrome, Schizophrenia

Status
Completed
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Metformin
Topiramate
Sponsored by
All India Institute of Medical Sciences, Bhubaneswar
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metabolic Syndrome focused on measuring Metabolic Syndrome, Schizophrenia, Atypical antipsychotics, Topiramate, Metformin

Eligibility Criteria

25 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Dept of Psychiatry, Aiims, Bhubaneswar

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Metformin arm

Topiramate arm

Arm Description

1000mg for 8 weeks

50mg for 8 weeks

Outcomes

Primary Outcome Measures

Change in the QRISK3 score.
QRISK3 (QRESEARCH cardiovascular risk algorithm)2018 algorithm- used for calculating the cardiovascular risk in the upcoming 10 years. It is measured for the age group of 25 to 84 years using information like age, weight, height, BMI, Lipid profile, past history of CKD, angina, migraine etc. Higher score indicates higher risk.

Secondary Outcome Measures

Change in the LDL/HDL ratio(Low density lipoprotein/High density lipoprotein).Higher ratio indicates higher risk
Calculated from the lipid profile
Change in Insulin Resistance (HOMA-IR)(homeostasis model assessment-estimated insulin resistance ).
Calculated from serum insulin level and fasting glucose level according to the Homeostatic Model Assessment of Insulin Resistance (HOMA-IR)
Change in Positive and negative syndrome scale
Positive and negative syndrome scale, a scale used to measure the symptom severity in patients of schizophrenia including positive, negative and general psychopathology.Higher scores indicate more severity of illness.Maximum score 30 and maximum 210
Change in Clinical Global Impression-Schizophrenia scale
Scale that is used to measure the baseline severity, change in severity of illness with treatment and global improvement. More score indicates more impairment.

Full Information

First Posted
December 4, 2021
Last Updated
August 21, 2023
Sponsor
All India Institute of Medical Sciences, Bhubaneswar
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1. Study Identification

Unique Protocol Identification Number
NCT05663749
Brief Title
Topiramate vs Metformin on Cardio-Metabolic Profile in Schizophrenia on Atypical Antipsychotics
Official Title
Efficacy and Safety of Add-on Topiramate vs Metformin on Cardio-Metabolic Profile in Patients With Schizophrenia on Atypical Antipsychotics With Metabolic Syndrome: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
September 20, 2022 (Actual)
Primary Completion Date
July 30, 2023 (Actual)
Study Completion Date
August 20, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
All India Institute of Medical Sciences, Bhubaneswar

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

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: PANSS: The Positive and Negative Syndrome Scale 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)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metabolic Syndrome, Schizophrenia
Keywords
Metabolic Syndrome, Schizophrenia, Atypical antipsychotics, Topiramate, Metformin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metformin arm
Arm Type
Active Comparator
Arm Description
1000mg for 8 weeks
Arm Title
Topiramate arm
Arm Type
Experimental
Arm Description
50mg for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Dibeta SR, Metgen, Glycomet
Intervention Description
1000mg for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Topiramate
Other Intervention Name(s)
Topamax, Topirol, Topaz
Intervention Description
50mg for 8 weeks
Primary Outcome Measure Information:
Title
Change in the QRISK3 score.
Description
QRISK3 (QRESEARCH cardiovascular risk algorithm)2018 algorithm- used for calculating the cardiovascular risk in the upcoming 10 years. It is measured for the age group of 25 to 84 years using information like age, weight, height, BMI, Lipid profile, past history of CKD, angina, migraine etc. Higher score indicates higher risk.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Change in the LDL/HDL ratio(Low density lipoprotein/High density lipoprotein).Higher ratio indicates higher risk
Description
Calculated from the lipid profile
Time Frame
8 weeks
Title
Change in Insulin Resistance (HOMA-IR)(homeostasis model assessment-estimated insulin resistance ).
Description
Calculated from serum insulin level and fasting glucose level according to the Homeostatic Model Assessment of Insulin Resistance (HOMA-IR)
Time Frame
8 weeks
Title
Change in Positive and negative syndrome scale
Description
Positive and negative syndrome scale, a scale used to measure the symptom severity in patients of schizophrenia including positive, negative and general psychopathology.Higher scores indicate more severity of illness.Maximum score 30 and maximum 210
Time Frame
8 weeks
Title
Change in Clinical Global Impression-Schizophrenia scale
Description
Scale that is used to measure the baseline severity, change in severity of illness with treatment and global improvement. More score indicates more impairment.
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Biswa Ranjan Mishra, MD, DPM
Organizational Affiliation
All India Institute of Medical Sciences, Bhubaneswar
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept of Psychiatry, Aiims, Bhubaneswar
City
Bhubaneswar
State/Province
Odisha
ZIP/Postal Code
751019
Country
India

12. IPD Sharing Statement

Plan to Share IPD
No
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Topiramate vs Metformin on Cardio-Metabolic Profile in Schizophrenia on Atypical Antipsychotics

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