Treatment-resistant Schizophrenia Clinical Trial
Official title:
An Exploratory Analysis of Immune and Inflammatory Response Associated With Clozapine Versus Non-Clozapine Antipsychotics in Individuals With Treatment-resistant Schizophrenia
The specific aim of this protocol is to compare Clozapine treatment vs Non-Clozapine antipsychotic treatment in a population of treatment-refractory individuals with schizophrenia. Specifically, it is to test if Clozapine leads to a decrease in levels of inflammatory markers, namely interleukin-6 but with an exploratory view of other markers. Clozapine has superior efficacy and is the only medication approved for treatment-refractory schizophrenia in addition to decreasing the risk of suicidal behavior as well. It is unclear why Clozapine has increased efficacy from a mechanistic viewpoint. We will look at the role of inflammatory markers and assess them 1x along with rating scales for psychosis and suicidality, the other entities which Clozapine has been shown to improve.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | June 2026 |
Est. primary completion date | March 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - All participants: - Between 18 and 65 years of age - Physically healthy (no clinically significant unstable medical condition as confirmed by medical history and physical examination) - Able to give informed consent - Treatment-Refractory Schizophrenia Clozapine treatment group (n = 30) Individuals treated with Clozapine consistently for a minimum of 6 months Non-Clozapine treatment group Continued treatment with non-Clozapine antipsychotic but would be eligible for Clozapine with the provider/patient electing to not pursue such for clinical reasons, consistently treated for at least 6 months Exclusion Criteria: - Clinically significant medical condition; cardiovascular, pulmonary, endocrine, or renal condition requiring in depth medical treatment - Active or recent (within 4 weeks) bacterial or viral infection - Chronic viral infection (hepatitis, HIV) - History of autoimmune, or chronic inflammatory condition - Current treatment with lithium - Treatment with Clozapine in the past 6 months - Current treatment with immunomodulatory or anti-inflammatory therapy - Vaccination within the past 3 months - Current alcohol or substance use disorder of moderate or severe severity - Intellectual disability (i.e. intelligence quotient <70) - Unwilling or unable to sign informed consent document - Pregnancy - Any patient deemed ineligible by PI discretion |
Country | Name | City | State |
---|---|---|---|
United States | Ohio State University Harding Hospital | Columbus | Ohio |
Lead Sponsor | Collaborator |
---|---|
Ohio State University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Interleukin-6 (IL-6) | Comparison in interleukin-6 between Clozapine and non-Clozapine group | Up to 1 year | |
Secondary | Other immune/cardiac markers | Comparison in hsCRP, interleukin-1ß, interferon-?, transforming growth factor-ß, tumor necrosis factor between Clozapine and non-Clozapine group | Up to 1 year | |
Secondary | Positive and Negative Syndrome symptom Scale | Comparison in psychosis rating scales (PANSS) between Clozapine and non-Clozapine group. Higher scores indicate more severe symptoms of psychosis. Score from 30-210 | Up to 1 year | |
Secondary | Self-injurious Thoughts and Behaviors Interviews | Comparison between Clozapine and non-Clozapine group in Suicidality rating scales. Scores on rating will be binary (yes/no) for suicidal ideation and also suicide attempts. | Up to 1 year |
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