Actively Recruiting
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
Eligibility Criteria
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
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
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Trial Site Locations
Total: 1 location
1
The Christie NHS Foundation Trust
Manchester, United Kingdom, M20 4BX
Actively Recruiting
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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