Status:
COMPLETED
Evaluation of MRI Sequences in Hepatic Overload
Lead Sponsor:
Rennes University Hospital
Conditions:
Iron and Fat Hepatic Overload
Eligibility:
All Genders
18+ years
Brief Summary
MRI, without any contrast injection, allows a non-invasive evaluation and quantification of hepatic overloads, especially iron (liver iron content LIC) and fat (steatosis) overloads, but in certain cl...
Eligibility Criteria
Inclusion
- Men and women ≥ 18 years of age
- Patients with or suspected clinically to be with a hepatic overload pathology (hepatic iron and/or fat overload) and who need a diagnostic or pre-therapeutic MRI from his initial management or during his monitoring,
- Patient able to provide written informed consent and can understand and comply with the requirements of the study
- Patient having received the information about the protocol and having not expressed his opposition to participate.
Exclusion
- Due to MRI :
- pacemaker or defibrillator,
- MRI non-compatible heart valve,
- clips, stents, coils, etc… non-compatible with MRI,
- cochlear implants,
- neuronal or peripheric simulator,
- intra-orbital or encephalic metallic foreign body, foreign body close to eyes, foreign body near the eyes, injury by metallic luster (war, ball),
- endoprosthesis received since less than 4weeks and osteosynthesis equipment received since less than 6 weeks,
- claustrophobia,
- pump, tattoo, permanent make-up, intrauterine device, patch,
- metal, magnetic, non-removable and in the area of the analyse field material
- Other criteria :
- unstable hemodynamic state, acute respiratory insufficiency, hemodynamically unstable acute respiratory failure, poor general condition or the necessity of a continuous monitoring incompatible with the MRI constraint,
- adults legally protected (under judicial protection, guardianship, or supervision), persons deprived of their liberty,
- pregnancy
Key Trial Info
Start Date :
March 4 2013
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 19 2018
Estimated Enrollment :
706 Patients enrolled
Trial Details
Trial ID
NCT01865461
Start Date
March 4 2013
End Date
December 19 2018
Last Update
March 11 2021
Active Locations (1)
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1
Rennes University Hospital
Rennes, France, 35033