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Optimization of MRI protocols in patients.

Optimization of MRI protocols in patients. - Optimization MRI protocols.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30773
Enrollment
400
Registered
2007-03-21
Start date
2007-04-01
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

géén van de bovenstaande, namelijk optimalisatie van MRI scan protocollen not applicable

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: informed consent age 18-65 years not known medical problems in contradiction with the study

Exclusion criteria

Exclusion criteria: - no informed consent - patients who are to ill - patients with claustrophobia - patients using medicaments which can influence the results of the study contra-indications for MRI - pregnancy

Design outcomes

Primary

MeasureTime frame
-enhancement of the signal-to-noise ratio and resolution -the decrease in scantime for specific sequences -enhancement of the detectability of specific pathologies.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)