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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00401336
Other study ID # DGS 2006/0197
Secondary ID PHRC/04-08CIC020
Status Completed
Phase N/A
First received
Last updated
Start date November 2006
Est. completion date March 2013

Study information

Verified date May 2023
Source Rennes University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Iron excess is increasingly regarded as an important cofactor in the morbidity attributed to many disorders. Assessment of body iron stores by measurement of serum ferritin concentrations has poor specificity and the most reliable method is histological or biochemical assessment from a liver biopsy. Because liver biopsy is an invasive procedure, imaging methods have been developed to detect and quantify hepatic iron content. The aim of the study is to use a simplified magnetic resonance imaging (MRI) technique to quantify simultaneously iron and fat contents in the liver and to compare the results to the quantification obtained biochemically.


Description:

Iron excess is increasingly regarded as an important cofactor in the morbidity attributed to many disorders. Assessment of body iron stores by measurement of serum ferritin concentrations has poor specificity and the most reliable method is histological or biochemical assessment from a liver biopsy. Because liver biopsy is an invasive procedure, imaging methods have been developed to detect and quantify hepatic iron content. The aim of the study is to use a simplified magnetic resonance imaging technique to quantify simultaneously iron and fat contents in the liver and to compare the results to the quantification obtained biochemically. Patients who need a liver biopsy will be proposed to be enrolled in the study. A magnetic resonance (MR) study will be performed using breath-hold gradient echo sequences with a single echo and a new multiple-echo gradient-echo sequence. Liver and muscle MR signal will be quantitatively determined and compared to biochemical assessment of liver iron concentration and steatosis quantification.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date March 2013
Est. primary completion date March 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adults over 18, - Planned liver biopsy (or liver biopsy within 2 months before inclusion) for one of these indications: suspicion of liver iron overload, metabolic syndrome, hepatitis B or C, alcohol abuse. No change in diet, transfusions or iron depletion must have occur between the liver biopsy and the MRI. - Having given a written informed consent. Exclusion Criteria: - Non cooperating patient, - Patient with dyspnea, - Patient with contra-indication to MR imaging (pace-maker, heart valve,...).

Study Design


Intervention

Device:
Magnetic resonance imaging multiecho gradient-echo sequence
Breath-hold gradient echo sequences with a single echo and a new multiple-echo gradient-echo sequence

Locations

Country Name City State
France CHU Angers Angers
France Hôpital Beaujon Clichy
France Hôpital Huriez Lille
France Hôpital Edouard Herriot Lyon
France Hôpital de la Timone Marseille
France Hôpital Saint Eloi Montpellier
France Hôpital Tenon Paris
France Hôpital de Pontchaillou Rennes
France Hôpital du Brabois Vandoeuvre les Nancy
Spain Hopital Donostia-San Sebastian San Sebastian

Sponsors (2)

Lead Sponsor Collaborator
Rennes University Hospital Ministry of Health, France

Countries where clinical trial is conducted

France,  Spain, 

References & Publications (3)

d'Assignies G, Paisant A, Bardou-Jacquet E, Boulic A, Bannier E, Laine F, Ropert M, Morcet J, Saint-Jalmes H, Gandon Y. Non-invasive measurement of liver iron concentration using 3-Tesla magnetic resonance imaging: validation against biopsy. Eur Radiol. 2 — View Citation

Paisant A, Boulic A, Bardou-Jacquet E, Bannier E, d'Assignies G, Laine F, Turlin B, Gandon Y. Assessment of liver iron overload by 3 T MRI. Abdom Radiol (NY). 2017 Jun;42(6):1713-1720. doi: 10.1007/s00261-017-1077-8. — View Citation

Paisant A, Laine F, Gandon Y, Bardou-Jacquet E. Is room temperature susceptometer really an accurate method to assess hepatocellular iron? J Hepatol. 2017 Dec;67(6):1345-1346. doi: 10.1016/j.jhep.2017.07.021. Epub 2017 Aug 5. No abstract available. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Liver to muscle signal intensity ratio and T2* calculation versus liver iron concentration during examination
Secondary Difference between in-phase and out-phase T2* calculation versus liver fat concentration during examination
Secondary Correlation between biochemical and MRI quantification of liver iron during examination
Secondary Correlation between participating centers during examination
Secondary Reproducibility of the multiecho gradient-echo sequence during examination
Secondary Influence of the antenna for the multiecho gradient-echo sequence during examination
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