Evaluation of a Support Software in the Planning and Real-time Monitoring of the Insertion of Needles in Interventional Magnetic Resonance Imaging (MRI): Liver Biopsy Case
Not Applicable
Terminated
- Conditions
- Liver Biopsy
- Registration Number
- NCT02573545
- Lead Sponsor
- University Hospital, Strasbourg, France
- Brief Summary
To demonstrate that the use of Standard @IFE and Planning@IFE features of the IFE software, compared to the current method, when planning and inserting the needle under MRI monitoring in the context of liver biopsies enable:
* a facilitation of the planning stages of the procedure (route path, marking of the entry point and alignment of the MRI cutaways on the planned path), resulting in a reduction in the duration of the planning stages,
* a facilitation of the real-time modification of MRI cutaways during the procedure, resulting in a reduction of the duration of the procedure
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 148
Inclusion Criteria
- Patient is at least 18 years old
- Affiliated to a social security scheme
- Informed consent
- Patient with an indication of liver biopsy eligible for a biopsy under interventional MRI
Exclusion Criteria
- Patient with a contraindication for MRI exam
- Patient with a contraindication for performing a biopsy
- Pregnancy
- Exclusion period
- Patient unable to receive and understand information about the study
- Patients under guardianship
- Patients under judicial protection
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Total duration of the intervention (planning and implementation) up to 2 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Nouvel Hôpital civil
🇫🇷Strasbourg, France
Nouvel Hôpital civil🇫🇷Strasbourg, France