CompletedNot Applicable

A Custom-Designed MR Coil for Spine Radiotherapy Treatment Planning

United States8 participantsStarted 2017-05-23

Plain-language summary

The purpose of this study is to assess the image quality improvement provided by a custom MR spine coil in comparison with the FDA approved coil when used for radiotherapy treatment planning.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Healthy Volunteers age 18 or older Exclusion Criteria: * Anyone who would be normally excluded from undergoing an MRI examination as per Memorial Hospital for Cancer and Allied Diseases Screening Questionnaire * Volunteers with a pacemaker, aneurysm clip or any other condition that would warrant avoidance of a strong magnetic field * Female volunteers who are pregnant or nursing * Volunteers who are unable to comply or complete the MRI exam due to claustrophobia or high levels of anxiety * Volunteers who are under direct supervision of any investigators on the study will not be eligible to participate

What they're measuring

Optimize performance

Timeframe: Day of intervention

Compare the signal-to-noise ratio of a custom spine coil with the existing FDA approved posterior coil array used for spine imaging

Timeframe: Day of intervention

Trial details

NCT IDNCT03170531

SponsorMemorial Sloan Kettering Cancer Center

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2021-04-26

View on ClinicalTrials.gov More Healthy trials