MRI Development for Radiotherapy Planning and Delivery in Non-Patient Volunteers
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age16+
SponsorThe Christie NHS Foundation Trust
About this trial
Non-patient volunteers will be scanned on the MR-Linac and MRSIM to facilitate the development, optimisation and validation of MRI protocols at The Christie NHS Foundation Trust.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Willing and able to provide written consent
Volunteers must undergo and satisfy MRI safety screening
Volunteers must be ≥ 16 years of age
Participants must agree to registration as a non-patient in CWP (the Trust's Electronic Health Record - EHR- system) and have their MRIs read and reported for incidental findings by a clinical radiologist
Disqualifiers
Any contraindications to MRI identified after MRI safety screening including completion of an MRI Safety Screening Form
Unable to tolerate MRI scan
Known Pregnancy
Known or suspected pathology in body region to be scanned
Trial population
Personnel at The Christie NHS Foundation Trust
Trial design
Design model
Other
Time perspective
Other
Treatments tested in this trial
Not listed
Trial groups
No trial groups listed
Trial outcomes
Primary outcomes
1
Developed and optimised of MRI scanning sequences for use in clinical radiotherapy practice in MR guided radiotherapy
on-going development of MRI protocols to be released for clinical use
Time frame
Through study completion - up to 5 yearsSponsors and contacts
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Source ClinicalTrials.gov