Role of Anti-Inflammatory Agents in Patients With Schizophrenia
Primary Purpose
Schizophrenia, Schizoaffective Disorder, Psychosis Not Otherwise Specified
Status
Completed
Phase
Phase 1
Locations
Pakistan
Study Type
Interventional
Intervention
Ondansetron
Simvastatin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Schizophrenia focused on measuring Anti inflammatory, Schizophrenia, Simvastatin, ondansetron
Eligibility Criteria
Inclusion Criteria:
- Diagnostic and Statistical Manual-IV (DSM-IV) diagnosis of schizophrenia, schizoaffective disorder, psychosis not otherwise specified or schizophreniform disorder
- competent and willing to give informed consent
- stable on medication 4 weeks prior to baseline
- able to take oral medication and likely to complete the required evaluations
- female participants of child bearing age must be willing to use adequate contraceptives for the duration of the study, and, willing to have a pregnancy test pre treatment and at ten weekly intervals while on study medication.
Exclusion Criteria:
- Relevant medical illness [renal and hepatic] in the opinion of the investigators
- history of high alcohol intake
- any change of psychotropic medications within the previous six weeks
- diagnosis of substance abuse (except nicotine or caffeine) or dependence within the last three months according to DSM-IV criteria
- pregnant or breast-feeding.
Sites / Locations
- Dow University of Health Sciences
- Karwan e hayat
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
Ondansetron
Simvastatin
Placebo
Arm Description
Outcomes
Primary Outcome Measures
acceptability and tolerability of simvastatin and ondansetron added to TAU
Secondary Outcome Measures
simvastatin and ondansetron added to TAU prevents the accumulation of negative symptoms in patients with schizophrenia
simvastatin and ondansetron added to TAU prevents cognitive decline
To compare the effect size
Full Information
NCT ID
NCT00929955
First Posted
June 28, 2009
Last Updated
August 2, 2019
Sponsor
Pakistan Institute of Living and Learning
Collaborators
Karwan e Hayat, Dow University of Health Sciences
1. Study Identification
Unique Protocol Identification Number
NCT00929955
Brief Title
Role of Anti-Inflammatory Agents in Patients With Schizophrenia
Official Title
Study of Role of Anti-Inflammatory Agents in Patients With Schizophrenia
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
June 2009 (Actual)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
September 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Pakistan Institute of Living and Learning
Collaborators
Karwan e Hayat, Dow University of Health Sciences
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
There is some evidence that anti-inflammatory treatment may have beneficial effects in schizophrenia and major depression. Cox-2 inhibitors have been tested in preliminary clinical trials for schizophrenia and depression, showing favourable effects compared to placebo (Muller and Schwarz et al 2009).
Statins were introduced as cholesterol-lowering agents but have found much wider usage. They are anti-inflammatory agents and thus similar to the Cox-2 inhibitors, which have shown some ability as adjuncts to improve the symptoms of schizophrenia in preliminary studies. The statins are also known to decrease C-reactive protein (CRP), which has been shown in an SMRI-funded study to be elevated in a study of individuals with schizophrenia. Fan et al (2007) demonstrated in a small study in patients with schizophrenia that higher than normal levels of CRP (>0.50 mg/dl) was associated with marked negative symptoms and higher total PANSS scores.
Ondansetron is a serotonin (5-HT3) receptor antagonist that is generic and widely used to prevent nausea and vomiting in patients receiving chemotherapy for cancer. GSK did a small study on it as an antipsychotic in the 1980s. Since then, several small studies have suggested that it is effective as an adjunct drug in improving the symptoms of schizophrenia.
Statins are widely used in schizophrenia sufferers, particularly those taking second generation antipsychotics, to treat hypercholesterolemia. Both drugs are well tolerated and their side effect profiles well understood.
We propose to conduct a feasibility study in patients with chronic schizophrenia to explore the adjunct use of simvastatin and ondansetron on positive, negative and general psychopathology in comparisons to treatment as usual (TAU) over a 12 week period.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Schizoaffective Disorder, Psychosis Not Otherwise Specified, Schizophreniform Disorder
Keywords
Anti inflammatory, Schizophrenia, Simvastatin, ondansetron
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
36 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Ondansetron
Arm Type
Active Comparator
Arm Title
Simvastatin
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Ondansetron
Intervention Description
ondansetron added to TAU Ondansetron will be administered in 8mg once daily dose
Intervention Type
Drug
Intervention Name(s)
Simvastatin
Intervention Description
Simvastatin added to TAU Simvastatin 20mg taken as once daily dose
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo added to TAU
Primary Outcome Measure Information:
Title
acceptability and tolerability of simvastatin and ondansetron added to TAU
Time Frame
3 months
Secondary Outcome Measure Information:
Title
simvastatin and ondansetron added to TAU prevents the accumulation of negative symptoms in patients with schizophrenia
Time Frame
3 months
Title
simvastatin and ondansetron added to TAU prevents cognitive decline
Time Frame
3 months
Title
To compare the effect size
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnostic and Statistical Manual-IV (DSM-IV) diagnosis of schizophrenia, schizoaffective disorder, psychosis not otherwise specified or schizophreniform disorder
competent and willing to give informed consent
stable on medication 4 weeks prior to baseline
able to take oral medication and likely to complete the required evaluations
female participants of child bearing age must be willing to use adequate contraceptives for the duration of the study, and, willing to have a pregnancy test pre treatment and at ten weekly intervals while on study medication.
Exclusion Criteria:
Relevant medical illness [renal and hepatic] in the opinion of the investigators
history of high alcohol intake
any change of psychotropic medications within the previous six weeks
diagnosis of substance abuse (except nicotine or caffeine) or dependence within the last three months according to DSM-IV criteria
pregnant or breast-feeding.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Imran B Chaudhry, MD
Organizational Affiliation
University of Manchester
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dow University of Health Sciences
City
Karachi
Country
Pakistan
Facility Name
Karwan e hayat
City
Karachi
Country
Pakistan
12. IPD Sharing Statement
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Role of Anti-Inflammatory Agents in Patients With Schizophrenia
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