MRI Development for Radiotherapy Planning and Delivery in Non-Patient Volunteers

The Christie NHS Foundation Trust500 enrolled

Overview

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.

Study Type

OBSERVATIONAL

Enrollment

500

Conditions

Focus of the Study is MRI Sequence Development

Eligibility

Sex: ALLMin age: 16 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * 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 Exclusion Criteria: * 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 * Member of study team

Locations (1)

The Christie NHS FT

Manchester, United Kingdom

RECRUITING

Outcomes

Primary Outcomes

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 years

Data from ClinicalTrials.gov

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