Schizophrenia Trial, Recruiting NCT06613334 Sponsor: Centre Hospitalier St Anne Condition: Schizophrenia
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Schizophrenia Trial, Recruiting

NCT06613334
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 are covered by a social security or other social protection scheme
  • People who have been diagnosed with schizophrenia according to the DSM-5 standard (diagnostic code F20)
  • People whose condition is currently in a stable state (no specific time period required for this stability)
  • People whose main antipsychotic medication is risperidone, paliperidone, aripiprazole, or olanzapine, taken either as a daily oral tablet or as a long-acting injectable
  • People who are also taking chlorpromazine, loxapine, or cyamemazine as an additional medication for anxiety or sedation
  • People who are able to speak and read French
  • People who are able to take part in speech-based assessments
  • People who are able to answer questionnaires on a smartphone
  • People who are under a legal guardianship or curatorship arrangement may still be considered
  • People who agree to take part and have signed an informed consent form, with a legal representative also signing if the person is under guardianship or curatorship

Who may not be able to join:

  • People who have a condition that affects their ability to use the French language
  • People who have a neurological condition such as multiple sclerosis, Parkinson's disease, Huntington's disease, or any other neurodegenerative disease
  • People who are currently taking lithium salts as part of their treatment
  • People who are currently taking anti-epileptic medication
  • People who are already taking part in another clinical trial that involves medication

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 27 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: Pierre De Maricourt, Dr, GHU Paris Psychiatry & Neurosciences

Phone: (0)1 45 65 86 91

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
Centre Hospitalier St Anne
Registry
ClinicalTrials.gov
Start date
4 October 2024
Est. completion
4 October 2026

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Voice interviews recorded on Callyope application; Plasma concentration of antipsychotics

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: 27 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