Schizophrenia Clinical Trial
Official title:
A Study Investigating the Relationship Between the Antipsychotic Response and Non-invasive Proxies of Neurochemistry in Schizophrenia
NCT number | NCT06159322 |
Other study ID # | 2021033 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | January 1, 2023 |
Est. completion date | January 30, 2024 |
The goal of this research project is to develop MRI-based biomarkers to identify patients with schizophrenia who are most likely to benefit from first-line antipsychotic or clozapine treatment. The MRI sequences (NM-MRI, MRS and rsfMRI) will be created by translating the best scientific evidence into a potential clinical product that has the highest chance of being clinically relevant predictor of treatment response. This study has the potential to significantly improve patient outcomes and reduce unnecessary interventions and costs at the Royal's Integrated Schizophrenia Recovery Program.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | January 30, 2024 |
Est. primary completion date | January 30, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 55 Years |
Eligibility | Inclusion Criteria: - Are voluntary and competent to consent to the study - Are between the ages of 18-55 - Are English literate - Have a diagnosis of schizophrenia or schizoaffective disorder - Are currently taking primarily olanzapine or clozapine Exclusion Criteria: - Medication for the treatment of schizophrenia or schizoaffective disorder has changed in the past month - Have a significant neurologic, neurodevelopmental, cardiovascular, renal, hepatic, hematological, gastrointestinal, pulmonary, or metabolic-endocrine disorder - Are pregnant or breastfeeding - Acquire positive urine test result for all drugs of abuse including cannabis - Have met DSM-5 criteria for substance use disorder other than tobacco in the last 6 months - Have a history of significant head trauma with loss of consciousness for more than 5 minutes - Have any contraindication to MRI - Have any other condition that in the opinion of the investigator(s) could create a hazard to the subject's safety, endanger the study procedures, or interfere with the interpretation of study results |
Country | Name | City | State |
---|---|---|---|
Canada | The Royal's Institute of Mental Health Research | Ottawa | Ontario |
Lead Sponsor | Collaborator |
---|---|
The Royal Ottawa Mental Health Centre | The Royal's Institute of Mental Health Research |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Neuromelanin-sensitive magnetic resonance imaging (MRI) contrast-to-noise ratio (CNR) | Indexes dopamine function | Will be examined cross-sectionally on an as-recruited basis. | |
Primary | Glutamate/glycine magnetic resonance sptrectroscopy (MRS) | Indexes glutamate & glycine concentration | Will be examined cross-sectionally on an as-recruited basis. |
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