Overview

Response to Clozapine in Treatment Resistant Schizophrenia: A Longitudinal Magnetic Resonance Spectroscopy Study

Status:
Recruiting
Trial end date:
2022-03-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to investigate the relationship between glutamate and related brain chemicals and treatment response to clozapine in patients with treatment-resistant schizophrenia.
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Centre for Addiction and Mental Health
Collaborator:
Canadian Institutes of Health Research (CIHR)
Treatments:
Clozapine
Criteria
Inclusion Criteria for Participants with TRS:

- DSM-IV/SCID diagnosis of schizophrenia, schizoaffective disorder, delusional disorder,
or psychotic disorder NOS.

- Age 18 years or older at time of scanning

- History of failure to respond to at least two previous sequential antipsychotic
treatments different to clozapine, each attaining a chlorpromazine daily dose of≥ 400
mg for a duration ≥ 6 consecutive weeks.Long-acting antipsychotic treatment will not
be allowed during the last trial prior to clozapine in order to avoid residual
concentrations or effects.Failure of treatment will be defined by a Clinical Global
Impression Severity (CGI-Severity) score of ≥4 and score of ≥4 on 2 Positive and
Negative Syndrome Scale (PANSS) positive symptom items. The CGI-Severity or Global
Assessment of Functioning (GAF) will be completed retrospectively based on information
provided by the participant, participant's psychiatrist, medical chart, or other
sources of available collateral information.

Exclusion Criteria for Participants with TRS:

- Incapacity to provide consent to participate in the research study.

- Substance abuse or dependence (within past six months), excluding nicotine and
caffeine.

- Positive urine drug screen for drugs of abuse.

- Metal implants or a pace-maker that would preclude the MRI scan.

- History of head trauma resulting in loss of consciousness > 30 minutes that required
medical attention.

- Unstable physical illness or significant neurological disorder including a seizure
disorder.

- Size of head, neck, and body being unable to fit MRI scanners.

- Refusal to provide consent to investigator to communicate with physician of record to
obtain collateral information.

- Psychiatric concerns raised by the physician of record regarding participation in the
study.

- Currently taking medications that may directly impact the glutamatergic system (i.e.
lamotrigine, topiramate, memantine or N-acetylcysteine)

- ECT, MST or TMS in the past 6 months

Inclusion criteria for Healthy Controls:

- Age of 18 and older at time of scanning

- Being capable to consent to study procedures

- Absence of history of psychiatric illness using the Mini-International
Neuropsychiatric Interview (MINI)

Exclusion criteria for Healthy Controls:

- First degree family member with primary psychotic disorder

- Substance abuse or dependence (within past six months), excluding nicotine and
caffeine.

- Positive urine drug screen for drugs of abuse

- Pacemakers, metallic cardiac valves, magnetic material such as surgical clips,
implanted electronic infusion pumps or any other conditions that would preclude the
MRI scan

- Clinically significant claustrophobia

- History of head trauma resulting in loss of consciousness > 30 minutes that required
medical attention

- Size of head, neck, and body being unable to fit MRI scanners

- Unstable physical illness or significant neurological disorder including a seizure
disorder