Schizophrenia Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are experiencing their first episode of psychosis and have been diagnosed with schizophrenia, schizoaffective disorder, schizophreniform disorder, or a similar psychosis condition according to standard diagnostic guidelines
- People who are currently experiencing moderate to severe symptoms such as hallucinations, unusual beliefs, feelings of grandiosity, or disorganised thinking, as measured by a standard rating scale
- People who have taken antipsychotic medication for no more than two weeks in total across their lifetime, placing them in the early stage of their illness
- People aged between 15 and 40 years old
- People who are already receiving, or are about to start, treatment with either aripiprazole or risperidone as part of their usual care
- People who have full ability to understand and agree to participate in the study
Who may not be able to join:
- People who choose to withdraw their consent to participate at any point during the study
- People who lose the ability to consent during the course of the study
- People whose treating psychiatrist decides they need a different antipsychotic medication other than aripiprazole or risperidone, for any reason including side effects or poor response
- People where the research team, study sponsor, or an independent safety committee decides it is necessary to remove them from the study for safety reasons
- People who are found to be pregnant during the study
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Juan Gallego, MD, Northwell Health
Phone: 949-486-9390
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Diagnostic performance of plasma NDE miRNA panel; Predictive performance of baseline plasma NDE miRNA levels for treatment response
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.