Testing of Radiofrequency Coil for Clinical 19F MRI

Testing of a dual tuned proton/fluorine MRI radio frequency coil

Images were collected from plastic fluorine phantoms taped to the upper thigh of health volunteers.

This trial was performed as part of an application for a Health Canada Investigational Device Exemption (Protocol # 226949)

Completed

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Key information

Conditions

Diagnostic Imaging

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Healthy Volunteer

Exclusion criteria

MRI incompatible patient
claustrophobia

Treatment and study plan

MRI

Device

Investigational device is a dual tuned (fluorine/proton) MRI surface coil designed and produced by Clinical MR solutions

Primary outcomes

Verify radio frequency coil imaging functionality on humans

Time frame: 1 hour of scanning

Proof of successful MRI signal acquisition with use of investigation device.
Measure signal repeatability in different patients

Time frame: 1 hour of scanning

MRI signal strength is expected to vary slightly based on patient weight.

Sponsors and collaborators

Lead sponsor

Western University, Canada

Other

Registry information

Important dates

Study start: 2015
Primary completion: 2015
Study completion: 2015
First posted: Feb 22, 2016
Registry last updated: Feb 22, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed