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7 Tesla MRI protocol development

Completed
Conditions
gezonde proefpersonen
control subjects/normal subjects
10022396
10015917
Registration Number
NL-OMON43914
Lead Sponsor
eids Universitair Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
400
Inclusion Criteria

Male and female subjects older than 18 years

Exclusion Criteria

All contra-indications for MRI (metal implants, claustrophobia, pacemaker, etc)
Pregnancy
Mentally disabled
Not having a general practitioner
For heatlhy control subjects: receiving medical treatment at the moment or in the year preceding the study.

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Improvements of scan techniques and development of new techniques are the main<br /><br>outcome of this study. These scans will be utilized in clinical research and<br /><br>patient care.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Small pilot studies performed for evaluation of image quality will be<br /><br>published.</p><br>
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