Testing of Radiofrequency Coil for Clinical 19F MRI

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02687750

Enrollment

Registered

2016-02-22

Start date

2015-01-31

Completion date

2015-12-31

Last updated

2016-02-22

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

Conditions

Diagnostic Imaging

Brief summary

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)

Interventions

DEVICEMRI

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

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

BASIC_SCIENCE

Masking

NONE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Yes

Inclusion criteria

* Healthy Volunteer

Exclusion criteria

* MRI incompatible patient * claustrophobia

Design outcomes

Primary

Measure	Time frame	Description
Verify radio frequency coil imaging functionality on humans	1 hour of scanning	Proof of successful MRI signal acquisition with use of investigation device.
Measure signal repeatability in different patients	1 hour of scanning	MRI signal strength is expected to vary slightly based on patient weight.

Outcome results

None listed

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