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Pharmacological and genetic imaging of executive function deficits

Pharmacological and genetic imaging of executive function deficits - Pharmacological and genetic imaging of executive function deficits

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON31059
Enrollment
80
Registered
2007-09-25
Start date
2007-10-01
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

psychische stoornissen: ontwikkelingsstoornissen (Autisme Spectrum Stoornissen) attention executive function deficits

Interventions

temporary, acute dopamine depletion by giving alpha-metyrosine (AMPT)

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 20 individuals with 22q11 deletion syndrome (DS) aged 18 till 40 years, 20 individuals with schizophrenia aged 18 till 40 years, 20 individuals with pervasive developmental disorder aged 18 till 40 years and 20 healthy volunteers, matched for age and gender, with no psychiatric history and no use of psychiatric medication.

Exclusion criteria

Exclusion criteria: Pregnancy and presence of metals that are not allowed in MRI-investigation

Design outcomes

Primary

MeasureTime frame
Blood Oxygen Level Dependant (BOLD) contrast measured during executive functioning tests within the MRI scanner

Secondary

MeasureTime frame
plasma levels of: * (HVA), * 3-methoxy-4 hydroxyphenethyleneglycol (MHPG), * VMA Urine levels of: * HVA * MHPG * VMA * dopamine * norepinephrine

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)