Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT04903236

MR-BIO: A Study to Evaluate Changes in MR Imaging and Biological Parameters

Led by University of Manchester · Updated on 2026-05-12

250

Participants Needed

1

Research Sites

323 weeks

Total Duration

On this page

Sponsors

U

University of Manchester

Lead Sponsor

T

The Christie NHS Foundation Trust

Collaborating Sponsor

AI-Summary

What this Trial Is About

The MR BIO study aims to understand the changes in the tumour and normal tissues during a course of radiotherapy. This is accomplished by studying the MR images taken during each treatment session on the MR Linear accelerator (MR Linac). The overarching hypothesis is that changes in MR imaging and biological parameters from blood, tissue, or urine biomarkers can be measured during radiotherapy and associated with clinical outcome. The MR Linac is a new radiotherapy machine with an on board MR scanner. This enables us to take images with high resolution and target the tumours more precisely and also reduce the dose to normal tissues. All patients undergoing treatment in the MR Linac at the Christie hospital will be considered for enrolment regardless of tumour site being treated. The study participants will receive the standard of care treatment for their disease condition. In addition, they will be requested to give weekly blood and urine samples during the course of radiotherapy and at first follow up. On completion of radiotherapy treatment, the participants will continue to be on standard of care follow up protocol with the treating oncologist. A small cohort of ten healthy volunteers will also be recruited to the study to develop and select some of the MR sequences only; they will not provide blood or urine samples. The healthy volunteers will be scanned for no more than one hour per session for a maximum of two sessions in total. These optimised sequences can then be used in the patient cohort.

CONDITIONS

Official Title

MR-BIO: A Study to Evaluate Changes in MR Imaging and Biological Parameters

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be willing and able to provide written consent
  • Be over 18 years of age
  • Undergo and satisfy MRI Safety Screening
  • Be under the care of a clinical oncologist at The Christie NHS Foundation Trust
  • Be planned to receive radiotherapy to the target site to be imaged
  • Be able to give blood and/or urine samples as required during treatment
  • Healthy volunteers must have no known or suspected significant medical condition
Not Eligible

You will not qualify if you...

  • Any condition that contraindicates MRI including failure to satisfy MRI Safety Screening Form
  • Presence of implanted pacemakers and/or pacing wires
  • Presence of cochlear implants
  • Presence of programmable hydrocephalus shunts
  • Presence of ferromagnetic implants
  • Unable to tolerate MR scans
  • Known HIV or active Hepatitis B or C infection
  • Pregnancy
  • Healthy volunteers must not be members of the study team

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Christie NHS Foundation Trust

Manchester, United Kingdom, M20 4BX

Actively Recruiting

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Research Team

R

Rachel Reed, MSc

CONTACT

K

Kimberley Reeves, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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