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Effects of Intranasal Insulin on Neuroimaging Markers and Cognition in Patients With Psychotic Disorders

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Mass General Brigham

Status and phase

Completed
Phase 2

Conditions

Bipolar I Disorder
Schizophrenia
Psychosis
Schizo Affective Disorder

Treatments

Drug: Intranasal Insulin

Study type

Interventional

Funder types

Other

Identifiers

NCT03943537
2019P000664

Details and patient eligibility

About

This clinical trial is a single center, single dose study of the acute effects of intranasal insulin on energy metabolism and cognitive function in patients with schizophrenia, schizoaffective and bipolar disorders, compared and healthy controls.

Full description

Psychotic disorders are common and severe psychiatric disorders. Despite advances in understanding the pathophysiology of these disorders, more effective and tolerable treatments are still needed. Evidence suggests that energy metabolism is altered in psychotic disorders. The investigators recently developed non-invasive MRI-based techniques to quantify redox balance and ATP generation in the brain. Targeting insulin pathways in the brain may allow for modulating abnormalities in energy metabolism. The investigators seek to examine whether intranasal insulin can modulate energy metabolism and improve cognition in patients with psychotic disorders. The study will use magnetic resonance spectroscopy (MRS) technology to measure in vivo energy metabolism processes in the brain, before and after the administration of intranasal insulin. Investigators will also measure changes in cognition with the administration of intranasal insulin.

Enrollment

87 patients

Sex

All

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Diagnostic and Statistical Manual of Mental Disorders (DSM) diagnoses of schizophrenia, schizoaffective disorder or bipolar disorder with psychotic features OR
  • Healthy Controls (no history of DSM psychiatric diagnoses, nor history of the same in first-degree relatives)

Exclusion criteria

  • Psychiatric hospitalization within the last 4 weeks
  • Unstable/active disease or potential contraindications, such as liver disease, kidney disease, uncontrolled hypertension, significant or unstable medical illness
  • Currently prescribed: antidiabetic agents, including oral antidiabetic medications and insulin, intranasal medication, steroids, weight loss agents
  • Pregnant or breast-feeding, not using an effective form of contraception for at least 3 months, and/or not abstinent for 1 month prior to enrollment
  • History of significant head injury
  • Contraindication to MRI scans (claustrophobia, cardiac pacemakers, metal clips and stents on blood vessels, artificial heart valves, artificial arms, hands, legs, etc., brain stimulator devices, implanted drug pumps, ear implants, eye implants or known metal fragments in eyes, exposure to shrapnel or metal filings, other metallic surgical hardware in vital areas, certain tattoos with metallic ink, certain transdermal patches, metal-containing IUDs).
  • Medical conditions preventing blood draws
  • History of electroconvulsive therapy (ECT) or transcranial magnetic stimulation (TMS) within the last 3 months
  • BMI > 35 or body weight > 350 lbs or BMI <18
  • DSM diagnosis of substance use disorder in the past month
  • For Healthy Controls:
  • Taking medication other than birth control

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

87 participants in 1 patient group

Intranasal Insulin (40 IU)
Experimental group
Description:
40 IU Novolin-R insulin will be administered one time using the ViaNase intranasal delivery device.
Treatment:
Drug: Intranasal Insulin

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Virginie-Anne Chouinard, M.D.; Jacey Anderson

Data sourced from clinicaltrials.gov

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