Phase
Condition
Tourette's Syndrome
Mood Disorders
Psychosis
Treatment
N/AClinical Study ID
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Males and females aged 18-65, in good general health based on history and physicalexamination
Psychiatrically healthy as determined by the Mini-International NeuropsychiatricInterview (M.I.N.I.PLUS) (94))
No relevant abnormalities in laboratory screening including thyroid function tests,blood cell count, serum electrolytes, liver and kidney function, and urinalysis
No clinically relevant findings in electrocardiography (ECG)
No clinically relevant findings in vital signs (blood pressure and pulse)
No regular use of illegal drugs or alcohol abuse based on declared history andconfirmed by urine drug screening
No history of repeated AMPH (AMPH), cocaine or other stimulant drug use
Exclusion
Exclusion Criteria:
Evidence of present psychiatric or neurological illness according to M.I.N.I.-Plus (any personal or first-degree relative history of: schizophrenia, bipolar disorder,attention-deficit/hyperactivity disorder, and substance dependence)
Recreational use of psychostimulant drugs in the past two years; lifetime use ofpsychostimulants exceeding five exposures
Medically significant biochemical or hematological abnormality on screening laboratorystudies
Women of childbearing potential: Current pregnancy or breast-feeding
Clinically relevant abnormalities in the electro-cardiogram (ECG)
History of myocardial infarction or angina pectoris
Positive urine drug screen within one week prior to PET study day
Presence of ferromagnetic metal in the body or heart pacemaker
Claustrophobia
Any history of arterial hypertension or paroxysmal hypertensive states
Established diagnosis of advanced arteriosclerosis
Established diagnosis of hyperthyroidism
History of hypersensitivity to sympathomimetics
History of head trauma resulting in loss of consciousness that required medicalintervention
Lifetime history of substance dependence (except nicotine)
If participation in this study would exceed the annual radiation dose limits (30 mSv)for human subjects
Subjects currently participating in research studies
Suicidal ideation or likelihood of a suicide or homicide attempt
Study Design
Study Description
Connect with a study center
Medical University of Vienna
Vienna, 1090
AustriaActive - Recruiting
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