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MRI protocol development at clinical field strengths

MRI protocol development at clinical field strengths - PROTO-MRI

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35342
Enrollment
500
Registered
2011-10-05
Start date
2011-07-27
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Gezonde vrijwilligers Healthy control subjects

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Healthy male and femal subjects older than 18 years and younger than 65 years

Exclusion criteria

Exclusion criteria: All contra-indications for MRI (metal implants, claustrophobia, pacemaker, etc Mentally disabled persons Under treatment of a medical specialist or under treatment of a medical specialist in the last year A chance of being pregnant (as reported by the volunteer) Not having a general practitioner Younger than 18 years Older than 65 years

Design outcomes

Primary

MeasureTime frame
Improvements of scan techniques and development of new techniques are the main outcome of this study. These techniques will be employed in clinical research and patient care.

Secondary

MeasureTime frame
Small pilot studies performed for evaluation and technical papers will be published.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)