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Studying brain energy and glutamate levels in schizophrenia using brain scans

Compares brain chemistry and activity scans in people with schizophrenia and healthy volunteers.

Plain-language title generated from the registry record
Registry title: Energetics and Glutamate in Schizophrenia

Key facts

Where
London, United KingdomSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT06236048, who can take part

Where in United Kingdom

  • South London and the Maudsley NHS Foundation TrustLondon, United KingdomTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
King's College London
Trial code
NCT06236048
Record updated
5 September 2025
Original description
The goal of this case-control study is to compare brain glutamate, glucose utilisation, lactate production and brain activity in healthy volunteers and people with a diagnosis of schizophrenia.Read full original descriptionShow less

Energetics and Glutamate in Schizophrenia

The goal of this case-control study is to compare brain glutamate, glucose utilisation, lactate production and brain activity in healthy volunteers and people with a diagnosis of schizophrenia.

It investigates the following main questions:

Whether, compared to healthy volunteers, participants with schizophrenia show:

1. reduction in brain glucose utilisation 2. increased brain lactate 3. greater variability in brain glutamate

Participants will be asked to have a screening visit, a MRI brain scan and a PET-MRI brain scan.

Inclusion: Healthy volunteer group:; No history of psychiatric illness, as assessed on the Mini neuropsychiatric Interview (MINI); Treatment responsive schizophrenia group:; Meeting ICD-11 criteria for schizophrenia (F20); Meeting symptomatic consensus criteria for remission, defined as scores of mild or less on items P1, P2, P3, N1, N4, N6, G5 and G9 of the PANSS and no history of symptomatic relapse in the past 6 months; Currently receiving one or more of the following antipsychotic medications: Olanzapine; Risperidone; Quetiapine; Amisulpride; Aripiprazole; Paliperidone; Antipsychotic adherent, defined as having a score of >=moderate adherence on the Kemp scale; Treatment-resistant schizophrenia group:; Meeting ICD-11 criteria for schizophrenia (F20); Meeting modified consensus criteria for treatment resistance, including history of at least two antipsychotic treatment trials each lasting ≥6 weeks at a dose of ≥400mg chlorpromazine equivalents; Total PANSS total score > 70; Moderate functional impairment (<60 on the SOFAS); Currently receiving one or more of the following antipsychotic medications: Clozapine; Olanzapine; Risperidone; Quetiapine; Amisulpride; Aripiprazole; Paliperidone; Antipsychotic adherent, defined as having a score of >=moderate adherence on the Kemp scale.

Exclusion: Severe claustrophobia prohibiting participation on PET or MRI 5. Body size above the comfortable limits for the MRI scanner. 6. Previous participation in research or clinical procedure/s involving ionising radiation, which, including the current study, would result in total radiation exposure >=10mSv within 12 months 7. History of head injury resulting in loss of consciousness for > 5 minutes 8. Meeting ICD-11 criteria for organic mental disorder (F00-F09) 9. Meeting ICD-11 criteria for mental and behavioural disorders due to psychoactive substance use (F10-F19) 10. With exclusion of nicotine or cannabis, meeting ICD-11 criteria for psychoactive substance dependence 11. Participation in clinical trial investigating any pharmacological agent other than a licensed antipsychotic compound in the last month; Diabetes or history of taking an antidiabetic medication 3. Presence of contraindication to MRI at 7 Tesla, including metallic or electronic implants and dental wires; All participants:; Pregnancy or breastfeeding; Lacking in mental capacity to provide informed consent to study participation.

ClinicalTrials.gov NCT06236048