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Recruiting NCT04749134

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

— Observational Focus of the Study is MRI Sequence Development

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Focus of the Study is MRI Sequence Development. Basic parameters: from 16 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United Kingdom
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

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.

Primary outcome measures

  • Developed and optimised of MRI scanning sequences for use in clinical radiotherapy practice in MR guided radiotherapy [Time frame: Through study completion - up to 5 years]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

United Kingdom · 1 center
  • The Christie NHS FT — Manchester

Identifiers

NCT: NCT04749134 · CFTSp170

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗