General Investigative MRI Protocol
Phase 1
- Conditions
- Multiple MRI Exams, IncludingCardiacAbdominalLumbarNeckPelvis
- Interventions
- Device: 16 Channel SPEEDER Flex Coil
- Registration Number
- NCT01598766
- Lead Sponsor
- Toshiba America Medical Systems, Inc.
- Brief Summary
This study is a feasibility study to evaluate new technology to improve the MRI experience, with coils, sequences and software. Patients from the Principle Investigator's exam schedule are given the opportunity to participate in this study is their MRI exam is appropriate for the specific coil, sequence or software being evaluated. If they agree, they can receive their MRI exam with the new coil, sequence or software instead of the standard one.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
- Pediatric patients that are scheduled for a clinically necessary MRI exam provided the subject meets the criteria of the department MRI screening procedure and their study is appropriate for the use of the 4 Channel Flex SPEEDER coil of the 16 Channel Metaflex SPEEDER coil.
Exclusion Criteria
- Any contraindication to MRI procedures
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Diagnostic Coil 16 Channel SPEEDER Flex Coil This coil is a lightweight, flexible coil which can be used for many pediatric MRI exams
- Primary Outcome Measures
Name Time Method 16 Channel Flex Coil May 2012-May 2013 The 16 Channel Flex Coil will be evaluated for how well it performs on pediatric patients.
- Secondary Outcome Measures
Name Time Method 8 Channel Value Breast Coil 6 months clinical evaluation to determine if an 8 channel mri breast coil meets industry standards.
Trial Locations
- Locations (1)
Steinberg Diagnostic Medical Imaging
🇺🇸Henderson, Nevada, United States