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Recruiting NCT05748990

NCT05748990 Does Abnormal Insulin Action in the Brain Underlie Cognitive and Metabolic Dysfunction in Schizophrenia

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Clinical Trial Summary
NCT ID NCT05748990
Status Recruiting
Phase
Sponsor Centre for Addiction and Mental Health
Condition Schizophrenia
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2023-04-01
Primary Completion 2026-08-01

Eligibility & Interventions

Sex All sexes
Min Age 17 Years
Max Age 45 Years
Study Type INTERVENTIONAL
Interventions
Intranasal insulinPlacebo

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 20 participants in total. It began in 2023-04-01 with a primary completion date of 2026-08-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Cognitive impairment (such as challenges in thinking and memory) is a core aspect of schizophrenia (SCZ), contributing to disability and poor functional outcomes. Additionally, almost half of the patients with SCZ are obese, the prevalence of type 2 diabetes is 3-6 times higher, and life expectancy is lower by 15-20 years compared to the general population. This is relevant as metabolic syndrome and diabetes are both associated with worse cognition among SCZ patients. Recent work studying the relationships between metabolic health and cognition has encouraged a new way of thinking about SCZ as both a metabolic and cognitive disorder. Brain insulin is involved in several processes relevant to SCZ, and abnormal brain insulin action may help explain both cognitive and metabolic abnormalities in patients with SCZ, but this has not been examined previously. Glucose uptake in several brain regions relevant to SCZ has been shown to be partially dependent on insulin. Therefore, in this study, the researchers will measure glucose uptake in the brain using an 18F-fluorodeoxyglucose (\[18F\]-FDG) positron emission tomography (PET) scan after an intranasal insulin stimulus, and will compare this measure between patients with SCZ and healthy controls.

Eligibility Criteria

Inclusion Criteria: i) Experimental group (participants with a diagnosis of schizophrenia spectrum disorder): 1. 17-45 years 2. both sexes; 3. Patients with first-episode schizophrenia spectrum illness: Primary DSM-5 diagnosis of schizophrenia, schizoaffective disorder, schizophreniform disorder, delusional disorder, brief psychotic disorder, psychotic disorder NOS, major depressive disorder with psychotic symptoms, bipolar I disorder, and bipolar II disorder, OR substance-induced psychosis, and antipsychotic treatment for schizophrenia, schizoaffective disorder, or other specified schizophrenia spectrum, other psychotic disorder, major depressive disorder with psychotic symptoms, bipolar I disorder, and bipolar II. (Diagnosis willbe confirmed via CAMH chart review). 4. BMI under or equal to 27 ii) Control group (healthy controls): 1. 17-45 years of age 2. sex-, 3. hand dominance -and 4. body mass index (BMI)-matched 5. Absence of DSM-5 diagnosis other than a specific phobia according to MINI Exclusion Criteria: 1. moderate or severe substance use according to MINI (per PI discretion in the case of moderate alcohol or cannabis use) 2. prediabetes, diabetes, or evidence of impaired glucose tolerance on screening OGTT 3. acute suicidal risk 4. use of weight, lipid, antidiabetic or blood pressure reducing agents 5. liver or kidney disease 6. pregnancy 7. nursing 8. pacemakers 9. metallic cardiac valves 10. magnetic material such as surgical clips, implanted electronic infusion pumps or any other conditions that would preclude the MRI scan 11. clinically significant claustrophobia (determined from MRI screening form; significance evaluated as per QI's discretion). 12. history of head trauma resulting in loss of consciousness \> 30 minutes that required medical attention; 13. size of head, neck, precluding to fit in the MRI or PET scanners 14. weight over 350lbs (limit for MRI scanner bed) 15. unstable physical illness 16. significant neurological disorder including a seizure disorder; 17. Received maximum allowed radiation in the past 12 months (20 mSv) 18. Completed more than 6 PET scans/ lifetime, that, together with the PET scanning procedures under this protocol will bring the total number of PET scans to more than the allowed/lifetime (8 PET scans per lifetime). These limits are set by the Centre for Addiction and Mental Health Brain Health Imaging Centre Guideline. 19. clinically relevant abnormality observed in medical history, 20. current intake of any medication that may interfere with participation in the study or may confound the results of PET imaging (e.g. anti-diabetic medication). 21. Disorders of coagulation, blood or ongoing use of anticoagulant medication Control group: Exclusionary criteria are as listed above for participants, in addition to: 1\) First degree family member with primary psychotic disorder.

Contact & Investigator

Central Contact

Mahavir Agarwal, MD, PhD

✉ mahavir.agarwal@camh.ca

📞 416-535-8501

Frequently Asked Questions

Who can join the NCT05748990 clinical trial?

This trial is open to participants of all sexes, aged 17 Years or older, up to 45 Years, studying Schizophrenia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05748990 currently recruiting?

Yes, NCT05748990 is actively recruiting participants. Contact the research team at mahavir.agarwal@camh.ca for enrollment information.

Where is the NCT05748990 trial being conducted?

This trial is being conducted at Toronto, Canada.

Who is sponsoring the NCT05748990 clinical trial?

NCT05748990 is sponsored by Centre for Addiction and Mental Health. The trial plans to enroll 20 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology