💬In plain words
What the trial is, and whether it could suit you
The aim of the present study is to detect changes in the dopamine system in the brain of patients with schizophrenia, especially when pretreated with antipsychotic medication. Here, the investigators want to find out whether the treatment with these drugs can cause permanent changes in docking points (receptors) of dopamine in the brain. It will be examined whether number and response of dopamine receptors is altered, which are associated with the onset of psychotic symptoms. For this purpose, a single PET/MR measurement will be performed in all participants. In total 140 volunteers, consisting of 30 healthy volunteers, 20 first-episode, drug-naive patients with schizophrenia and 90 pretreated patients with schizophrenia will be included over a time period of three years. In addition, the influence of nicotine consumption on dopamine receptors will be invesitgated by comparing data from
Sign in to get the eligibility rules as simple questions to take to your doctor.
📋 Eligibility rules (as published)
Inclusion Criteria for healthy subjects:
* Age: 18-65
* The subject is capable to understand scope and individual consequences of the clinical study.
* An informed consent is signed and personally dated by the subject. • No psychiatric disorder (DSM-5) currently, or in the medical history (ensured by a standardized psychiatric interview Mini International Neuropsychiatric Interview (M.I.N.I.)).
Inclusion Criteria for patients:
* Age: 18-65
* The criteria for schizophrenia after DSM-5 are met.
* The subject is capable to understand scope and individual consequences of the clinical study.
* For first-episode patients, no application of antipsychotic drugs in history. Other psychoactive substances (in particular antidepressants) are allowed if last application is at least three months ago and total Duration did not exceed three months. Benzodiazepines are allowed.
* For medically pretreated patients: at least one year pharmacotherapy with one of the following three substances: aripiprazole or quetiapine or risperidone. A medication break of - depending on the plasma level - two days (quetiapine) up to two weeks (aripiprazole) should be clinically defensible.
* An informed consent is signed and personally dated by the patient. For patients with legal support in addition: signature of the legal supervisor.
Exclusion criteria for patients and subjects:
* Hypersensitivity against apomorphine or a chemically similar substance or one of the components of the applied medication.
* Participation in other clinical trials during or within six months prior to this clinical study.
* Medical or psychological conditions which may endanger a proper performance of the clinical trial.
* Physical disorders which interfere according to type and severity with the planned examinations, which could influence the parameter to be investigated or could compromise the subject during the examination procedure.
* Inability to comply with the study protocol.
* Limited or completely repealed legal capacity.
* For female participants: positive pregnancy test on the day of the study inclusion or on the day of the PET/MR-measurement.
* Acute suicidality or endangerment
* Poor general condition.
* Participation in a study using ionising Radiation within the last five years.
* Alcohol abuse, alcohol dependence or addiction disease / abuse of dependence-inducing substances (excluding nicotine) in the history, additional exclusion criterion for healthy subjects: regular medication intake; within the last two weeks before PET/MR-measurement no drugs at all must be taken.
Additional exclusion criterion for patients: other than the approved axis I diagnosis according to DSM-5. An axis II diagnosis is not a criterion for exclusion
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