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Clinical Trial Summary

This study therefore aims to assess current treatment recommended by scientific societies [ 6-13 ] , brain MRI with injection of contrast for the diagnosis and monitoring of brain metastases . The recommended dose of this examination gadolinium is from 0.1 to 0.3 mmol / kg [ 14 ] . Sequences infusion different from one center to the other made : some use the infusion T1, other infusion T2 * . No recommendation establishes whether it is preferable to use one or the other of these sequences.

No examination is added for the purposes of protocol. Indications for MRI and the number and timing of MRI checks under this protocol are consistent with what is done in practice . The used type of gadolinium and the injected dose will be identical for both sequences infusion . The assessment shall not in any case the contrast but the interpretation of the sequence itself. Special procedures monitoring implemented embodiment correspond to the two sequences instead of infusion (one of T1-weighted and T2 * in the other ) , in the original MRI and MRI of the first control , in order to compare their effectiveness


Clinical Trial Description

Eligibility criteria:

- Major Patients

- Addressed MRI for initial assessment of brain metastases

- At a suspicion of one or more brain metastases in the brain scanner routine screening

- Follow for lung cancer histologically documented

- In the Thoracic Oncology Service Professor Lafitte (contact: Dr Cortot)

- To whom treatment with chemotherapy or targeted therapy (including anti-angiogenic) is considered

- Be socially insured

Main Outcomes measures:

Comparing the area under the ROC curve of different parameters evaluated in T1 and T2 * perfusion during the initial assessment for the diagnosis of maximal tumor response evaluated at 1 year ;


Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT02250755
Study type Interventional
Source University Hospital, Lille
Contact
Status Completed
Phase N/A
Start date June 2013
Completion date November 2015