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The influence of antipsychotic medication on dopamine D2 receptor availability. A [11C] raclopride PET study

The influence of antipsychotic medication on dopamine D2 receptor availability. A [11C] raclopride PET study - Hamlett PET-study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55703
Enrollment
45
Registered
2018-04-30
Start date
2019-01-03
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

dopamine psychosis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: * The participant understands the study and is able to provide written informed consent * Must be between the ages of 18-60 * Sufficient command of the Dutch language * Must have a diagnosis of schizophrenia, schizoaffective disorder, schizophreniform disorder, or those classified as Other Specified Schizophrenia Spectrum and Other Psychotic Disorder * Be mentally competent, as determined by their treating physician * The participant has had a first episode of psychosis and uses antipsychotic medication at the start of the HAMLETT study * The participant is about to discontinue antipsychotic medication * Psychotic symptoms are in remission for 3-6 months * HAMLETT is the only medical-scientific medication study in which the patient participates

Exclusion criteria

Exclusion criteria: * Presence of a neurological disorder * Visual or hearing problems that cannot be corrected * Participation in a scientific research study during the past year involving radiation * the refusal to be informed (by notifying the participant*s physician) of structural brain abnormalities that could be detected during the experiment * MR incompatible implants in the body * Risk of having metal particles in the eyes * Tattoo*s containing red pigments that form a safety risk * Alcohol or substance abuse in the past 6 months * Insufficient knowledge of the Dutch language * Inability to undergo cognitive testing * Use of antipsychotic medication * dangerous or harmful behaviour (i.e. behaviour with a risk of severe physical injury, or actual physical injury inflicted, to self or others) occurred during the psychosis * Coercive treatment (based on a judicial ruling)

Design outcomes

Primary

MeasureTime frame
The main study parameter is be the binding potential of [11C]raclopride in the striatum (caudate and putamen).

Secondary

MeasureTime frame
n.a.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)