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General Investigative MRI Protocol

NCT01598766 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2013-02-05

No results posted yet for this study

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.

Conditions

  • Multiple MRI Exams, Including
  • Cardiac
  • Abdominal
  • Lumbar
  • Neck
  • Pelvis

Interventions

DEVICE

16 Channel SPEEDER Flex Coil

This is a 16 element MRI coil, flexible, lightweight. Multiple uses.

Sponsors & Collaborators

  • Toshiba America Medical Systems, Inc.

    lead INDUSTRY

Principal Investigators

  • Mark L Winkler, MD · Steinberg Diagnostic Medical Imaging

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
6 Months
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2013-05-31
Completion
2020-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01598766 on ClinicalTrials.gov