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:
(For people being assessed for a first episode of psychosis)
- People who have received a diagnosis (assessed using a standard psychiatric tool called DSM-IV) of one of the following: schizophrenia, schizophreniform psychosis, psychosis not otherwise specified (NOS), brief psychosis, schizoaffective syndrome, or delusional disorder
- People who have been taking antipsychotic medication for less than 4 weeks before joining the trial
(For healthy comparison participants)
- People with no personal history of a major psychiatric disorder, including no history of substance use disorders
- People with no family history of psychotic disorders in close blood relatives (parents, siblings, or children)
Who may not be able to join:
(For people being assessed for a first episode of psychosis)
- People whose psychotic symptoms are primarily related to another dominant psychiatric illness
(For all participants)
- People with a significant physical health condition, or a past or current condition affecting the brain (such as a brain tumour, neuroinflammatory disease, or epilepsy), based on medical history, physical signs, MRI results, or laboratory tests
- People who have been exposed to a significant level of medical radiation (25 mSv or more) in the past year
- Women who are pregnant, breastfeeding, or currently lactating
- People who meet the diagnostic criteria for a substance use disorder (not including nicotine dependence), based on DSM-IV assessment or repeated positive drug tests during the study
- People with any metallic object in the eye, or with certain metallic or electromagnetic implants in the body, or who have experienced claustrophobia (fear of enclosed spaces) during an MRI scan
- People who have had symptoms of a severe bacterial, fungal, or viral infection — including upper respiratory infections with effects on the whole body such as fever — within the 7 days before joining
- People who have taken blood-thinning (antihemostatic) medication within 2 weeks before certain procedures involved in the study (a lumbar puncture and arterial line placement)
- People who have donated blood (one unit or more) in the 90 days before initial screening, plasma in the week before screening, or platelets in the 6 weeks before joining
- People who, for any other reason, the trial investigators or sponsor consider unsuitable — this may include very severe symptoms or signs of aggression or hostility
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
Phone: +46 702127287
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
Kynurenic acid (KYNA) in FEP compared to HC; Cytokines in FEP compared to HC; Microglial activation in FEP compared to HC; Dopamine receptors in FEP compared to HC; Infectious risk factors in FEP and subsequent relation to clinical outcome
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.