Schizophrenia Trial, Recruiting NCT05763966 Sponsor: Uppsala University Condition: Schizophrenia
Back to Schizophrenia

Schizophrenia Trial, Recruiting

NCT05763966
Recruiting Not Applicable

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 have been diagnosed (using DSM-5 criteria) with one of the following: schizophrenia, schizophreniform psychosis, psychosis not otherwise specified, brief psychosis, schizoaffective syndrome, or delusional disorder — and whose psychotic symptoms and decline in day-to-day functioning began no more than 3 years before joining the study (Early Psychosis group)
  • People who have been assessed using a specialised interview tool (called SIPS) and identified as being at clinical high risk of developing psychosis (High Risk group)

Who may not be able to join:

  • People (in the Early Psychosis or High Risk groups) whose main psychiatric diagnosis is considered to be the cause of their psychotic symptoms — for example, bipolar disorder, major depressive disorder, or autism
  • People (in the Early Psychosis or High Risk groups) who have been taking benzodiazepine medications daily for more than two weeks and would be unable to pause that treatment during the study's testing procedures
  • People joining as healthy comparison participants who have ever been diagnosed with a major psychiatric disorder, including substance use disorders
  • People joining as healthy comparison participants who have a parent, sibling, or child with a history of a psychotic disorder or bipolar disorder
  • People with a significant physical health condition, or a past or current condition affecting the brain (such as a brain tumour, neuroinflammatory disease, epilepsy, or significant brain injury), based on medical history, physical signs, MRI, or lab results
  • People who have been exposed to a radiation dose of 25 mSv or more in the past year
  • Women who are pregnant, breastfeeding, or lactating
  • People who are not sufficiently proficient in Swedish, or who have a documented intellectual disability that would prevent them from giving informed consent
  • People who meet the DSM-5 diagnostic criteria for a substance use disorder (not including nicotine dependence), or who have repeated positive drug screening results during the study
  • People with a metallic object in the eye, ferro/electromagnetic implants, or a history of claustrophobia during MRI scans
  • People who have had symptoms of a severe bacterial, fungal, or viral infection with whole-body effects (such as fever) within the 7 days before joining
  • People who have taken blood-thinning medications within 2 weeks before certain study procedures (lumbar puncture and arterial line placement) at either the start of the study or the one-year follow-up
  • People who have donated blood (one unit or more) within the past 90 days, donated plasma within the past week, or donated platelets within the past 6 weeks before screening
  • People considered unsuitable for other reasons at the discretion of the study investigator or sponsor — 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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 14 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Simon Cervenka, MD, PhD, Uppsala University

Phone: +46709944226

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Uppsala University
Registry
ClinicalTrials.gov
Start date
1 April 2023
Est. completion
31 December 2026

Where this trial is recruiting

🇸🇪 Sweden

Primary endpoints

Synaptic density in early stage psychosis (EPP) patients and individuals at Clinical High Risk for Psychosis (CHR-P) compared to healthy controls (HC).; Changes in synaptic density in EPP and CHR-P between baseline and after 1 year.; Measures of cognitive function, magnetic resonance imaging (MRI), electroencephalogram (EEG) in relation to SV2A in EPP, CHR-P and HC.; Measures of cognitive function, magnetic resonance imaging (MRI), electroencephalogram (EEG) in relation to changes in SV2A in EPP and CHR-P.; Candidate disease markers in cerebrospinal fluid in relation to SV2A in EPP, CHR-P and...

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov