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 have been diagnosed with schizophrenia (according to a standard medical classification system called DSM-5), have a symptom severity score above a certain level, and whose schizophrenia has not responded to a medication called clozapine — either because the medication did not work, they could not tolerate it, or it was not safe for them to take it.
Who may not be able to join:
- People who have a diagnosis of dementia or significant memory and thinking problems, a current serious substance use disorder, mood disorders that include psychotic symptoms, or a personality disorder.
- People who are not able to read or write in German.
- People who are pregnant or currently breastfeeding.
- People who have a general health condition that means it would not be safe for them to receive electroconvulsive therapy (ECT), a medical treatment involving brief electrical stimulation of the brain (confirm with trial site for details on what conditions apply).
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: Alexander Sartorius, Prof, Central Institute of Mental Health (CIMH), Mannheim, Germany
Phone: +49-621-1703
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
Time to relapse
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.