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General Investigative MRI Protocol

General Investigational Protocol for EXCELART VANTAGE ZGV/XGV/AGV/ ATLAS/XGV/ZGV TITAN/XGV VANTAGE TITAN 3T

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01598766
Enrollment
100
Registered
2012-05-15
Start date
2012-05-31
Completion date
2020-05-31
Last updated
2013-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

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.

Interventions

DEVICE16 Channel SPEEDER Flex Coil

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

Sponsors

Toshiba America Medical Systems, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to 18 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
16 Channel Flex CoilMay 2012-May 2013The 16 Channel Flex Coil will be evaluated for how well it performs on pediatric patients.

Secondary

MeasureTime frameDescription
8 Channel Value Breast Coil6 monthsclinical evaluation to determine if an 8 channel mri breast coil meets industry standards.

Countries

United States

Contacts

Primary ContactErin Kelly
ekelly@tams.com7146046242

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026