General Investigative MRI Protocol

Toshiba Medical Systems

Status and phase: Unknown; Phase 1

Conditions: Abdominal; Neck; Cardiac; Multiple MRI Exams, Including; Pelvis; Lumbar

Treatments: Device: 16 Channel SPEEDER Flex Coil

Study type: Interventional

Funder types: Industry

Identifiers

NCT01598766

05069

Details and patient eligibility

About

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.

Enrollment: 100 estimated patients

Sex: All

Ages: 6 months to 18 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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100 participants in 1 patient group

Diagnostic Coil

Experimental group

Description:

This coil is a lightweight, flexible coil which can be used for many pediatric MRI exams

Treatment:

Device: 16 Channel SPEEDER Flex Coil