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Methodological Developments for Magnetic Resonance Imaging (MRI) (METHODO)

C

Central Hospital, Nancy, France

Status

Completed

Conditions

Healthy Subjects

Treatments

Device: MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT02887053
2008-A01209-46

Details and patient eligibility

About

The purpose of this study is to optimize clinical MR protocols and to validate MR acquisition parameters.

Enrollment

1,807 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • to be over 18 year-old,
  • to be able to give an informed consent,
  • to have underwent a pre-inclusion medical examination,
  • to present no contraindication to MR examination,
  • to be enrolled in a social security plan.

Exclusion criteria

  • subject refusal,
  • subject under a measure of legal protection,
  • any contraindication to MR examination (active medical device, ferromagnetic foreign body, pregnancy, morbid obesity, claustrophobia, ... ).

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1,807 participants in 1 patient group

All subjects
Experimental group
Description:
All subjects will have an MRI examination
Treatment:
Device: MRI

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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