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Mapping dopaminergic function using pharmacologic Magnetic Resonance Imaging (phMRI)

Mapping dopaminergic function using pharmacologic Magnetic Resonance Imaging (phMRI) - Dopamine-MRI

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON33010
Enrollment
10
Registered
2009-05-18
Start date
2009-03-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

kinder en jeugd psychiatrie not applicable

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Healthy male adult volunteers, aged between 20 and 35.

Exclusion criteria

Exclusion criteria: Contraindications for MRI (e.g. osteosynthetic material, pacemaker, artificial cardiac valves); claustrophobia. Symptomatic cardiovascular disease, moderate-to-severe hypertension, hyperthyroidism, glaucoma, hypersensitivity or idiosyncrasy to sympathomimetic amines, agitation, and history of drug abuse, or use of psychotropic drugs that affect DA function, such as methylphenidate and cocaine (anamnestic). Finally, cardial conduction disorder (abnormal ECG) en renal disease (serum creatinine * 110 mmol/L).

Design outcomes

Primary

MeasureTime frame
BOLD: % change in BOLD SI from baseline (ROI) PWI: % change in ratio from baseline (ROI: rCBV/white matter rCBV) ASL: % change in CBF from baseline (ROI CBF/100 mg tissue) SPECT: DAT ratio (striatal ROI binding/binding in cerebellum)

Secondary

MeasureTime frame
Amphetamine Interview Rating Scale

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)