CTRI Number |
CTRI/2019/05/019447 [Registered on: 30/05/2019] Trial Registered Prospectively |
Last Modified On: |
28/05/2019 |
Post Graduate Thesis |
Yes |
Type of Trial |
Observational |
Type of Study
|
Cross Sectional Study |
Study Design |
Non-randomized, Multiple Arm Trial |
Public Title of Study
|
A STUDY TO COMPARE THE WEIGHT, BLOOD SUGAR AND FAT CHANGES IN PATIENTS ON TREATMENT WITH OLANZAPINE, RISPERIDONE AND QUETIAPINE. |
Scientific Title of Study
|
“A CROSS-SECTIONAL STUDY TO COMPARE THE METABOLIC ADVERSE EFFECTS IN PATIENTS RECEIVING TREATMENT WITH OLANZAPINE OR RISPERIDONE OR QUETIAPINE." |
Trial Acronym |
|
Secondary IDs if Any
|
Secondary ID |
Identifier |
NIL |
NIL |
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
Name |
Dr Quadros Reshma Ronald |
Designation |
Postgraduate Resident |
Affiliation |
Father Muller Medical College Hospital |
Address |
Department of Pharmacology,
Block - A,
Father Muller Medical College,
Kankanady, Mangalore
Kankanady,
Mangalore- 575002.
Karnataka Dakshina Kannada KARNATAKA 575002 India |
Phone |
9620792441 |
Fax |
|
Email |
reshmaquadros.rq@gmail.com |
|
Details of Contact Person Scientific Query
|
Name |
Dr Padmaja Udaykumar |
Designation |
Professor and Head of Department |
Affiliation |
Father Muller Medical College Hospital |
Address |
Department of Pharmacology,
Block - A,
Father Muller Medical College,
Kankanady, Mangalore
Kankanady,
Mangalore- 575002.
Karnataka Dakshina Kannada KARNATAKA 575002 India |
Phone |
9880890512 |
Fax |
|
Email |
padmajaudaykumar@gmail.com |
|
Details of Contact Person Public Query
|
Name |
Dr Quadros Reshma Ronald |
Designation |
Postgraduate Resident |
Affiliation |
Father Muller Medical College Hospital |
Address |
Department of Pharmacology,
Block - A,
Father Muller Medical College,
Kankanady, Mangalore
Kankanady,
Mangalore- 575002.
Karnataka Dakshina Kannada KARNATAKA 575002 India |
Phone |
9620792441 |
Fax |
|
Email |
reshmaquadros.rq@gmail.com |
|
Source of Monetary or Material Support
|
Father Muller Medical Hospital,
Kankanady, Mangalore- 575002 |
|
Primary Sponsor
|
Name |
Father Muller Medical College Hospital |
Address |
Kankanady, Mangalore - 575002 |
Type of Sponsor |
Private medical college |
|
Details of Secondary Sponsor
|
|
Countries of Recruitment
|
India |
Sites of Study
|
No of Sites = 1 |
Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
Dr Quadros Reshma Ronald |
Father Muller Medical Hospital |
Psychiatry OPD (OPD No.66) and wards (Psychiatry ward- 90), Father Muller Medical Hospital,Kankanady,Mangalore. Dakshina Kannada KARNATAKA |
9620792441
reshmaquadros.rq@gmail.com |
|
Details of Ethics Committee
|
No of Ethics Committees= 1 |
Name of Committee |
Approval Status |
Father Muller Medical College Institutional Ethics Committee |
Approved |
|
Regulatory Clearance Status from DCGI
|
|
Health Condition / Problems Studied
|
Health Type |
Condition |
Patients |
(1) ICD-10 Condition: F01-F99||Mental, Behavioral and Neurodevelopmental disorders, |
|
Intervention / Comparator Agent
|
Type |
Name |
Details |
Intervention |
NIL |
NIL |
|
Inclusion Criteria
|
Age From |
20.00 Year(s) |
Age To |
65.00 Year(s) |
Gender |
Both |
Details |
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.
|
|
ExclusionCriteria |
Details |
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).
|
|
Method of Generating Random Sequence
|
Not Applicable |
Method of Concealment
|
Not Applicable |
Blinding/Masking
|
Not Applicable |
Primary Outcome
|
Outcome |
TimePoints |
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. |
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 Outcome
|
Outcome |
TimePoints |
To assess the Blood pressure change from baseline in patients receiving treatment with olanzapine or risperidone or quetiapine. |
Patients will be assessed at that time point when on treatment with the study drugs for a duration of 6 months to 1 year. |
|
Target Sample Size
|
Total Sample Size="86" Sample Size from India="86"
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" |
Phase of Trial
|
N/A |
Date of First Enrollment (India)
|
01/06/2019 |
Date of Study Completion (India) |
Applicable only for Completed/Terminated trials |
Date of First Enrollment (Global) |
Date Missing |
Date of Study Completion (Global) |
Applicable only for Completed/Terminated trials |
Estimated Duration of Trial
|
Years="1" Months="0" Days="0" |
Recruitment Status of Trial (Global)
|
Not Applicable |
Recruitment Status of Trial (India) |
Not Yet Recruiting |
Publication Details
|
NIL |
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
|
Brief Summary
|
OBJECTIVES OF THE STUDY: To study the adverse effects on metabolic parameters in patients receiving treatment with either Olanzapine or Quetiapine or Risperidone. NEED FOR THE STUDY: Head to head Comparison of Metabolic disturbance induced by Olanzapine, risperidone and quetiapine is a little researched domain and there is a distinct lack of information in this aspect, particularly in Indian subjects. There is a need to look into the association of dose and duration of treatment with study drugs and the risk of developing metabolic adverse drug effects, so as to intervene at that point to prevent unfavorable outcome. As early onset diabetes and associated cardiometabolic complications are on the rise in general population in India, it is pertinent to study the occurrence of metabolic abnormalities like hyperglycemia, dyslipidemia and obesity in patients on monotherapy with study drugs thus contributing to the appropriate drug choices these patients requiring antipsychotic therapy. MATERIAL AND METHODS STUDY TYPE: Observational, hospital based study. SOURCE OF DATA: Inpatients and Outpatients attending the Department of Psychiatry , Father Muller Medical College Hospital , Mangalore will be screened for inclusion based on the criteria given below. SELECTION 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. · Patients of either gender aged between 20-65 yrs. 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). METHOD OF COLLECTION OF DATA This is a cross-sectional, observational study in which patients taking antipsychotic treatment prescribed to them by their treating psychiatrist, for a minimum period of 6 months to a maximum period of 1 year and fulfilling the above mentioned criteria will be recruited for the study. A written informed consent will be taken before proceeding to assess the metabolic parameters. Baseline data like psychiatric diagnosis, height, weight and blood pressure before the initiation of therapy, prescribed drugs, dose and duration of treatment with the study drugs will be taken from case records. A detailed patient history will be taken covering the following categories: Patient details, Clinical history, family and personal history, treatment information including current antipsychotic, dose and duration of treatment, previous anti-psychotic treatment, will be collected. Clinical examination for signs of insulin resistance , dyslipidemia, vitals like blood pressure and anthropometric measurements like weight, height, BMI will be obtained from all participants . The subjects will then be assessed for the present analyses which includes laboratory investigations like fasting blood samples for plasma glucose , whole blood glycated HbA1c, Serum Triglycerides and serum HDL. All the blood tests will be done according to the same standardized procedures of Father Muller Medical Hospital , Mangalore laboratory. All the details obtained will then be entered into a predesigned Proforma and analyzed statistically. |