Focus of the Study is MRI Sequence Development
Conditions
Brief summary
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.
Interventions
None listed
Sponsors
The Christie NHS Foundation Trust
Study design
Observational model
OTHER
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Developed and optimised of MRI scanning sequences for use in clinical radiotherapy practice in MR guided radiotherapy | Through study completion - up to 5 years | on-going development of MRI protocols to be released for clinical use |
Countries
United Kingdom
Outcome results
None listed