Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06965101

Rapid Response MRI-Guided Palliative Radiotherapy for Urgent Treatment of Metastatic Spinal Cord Compression Compared to Standard Radiotherapy Pathway

Led by The Christie NHS Foundation Trust · Updated on 2025-12-02

72

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether the Magnetic Resonance Linear Accelerator (MRL) can speed up radiotherapy treatment for patients with Metastatic Spinal Cord Compression (MSCC). The study aims to see if treatment can be successfully delivered in a single one-hour appointment on the MRL compared to the standard care pathway requiring two separate visits: a planning CT scan and a radiotherapy appointment. The trial also explores whether treatment with the MRL can be given within 24 hours from the decision to treat and assesses patient satisfaction through questionnaires. Participants will receive radiotherapy with a prescribed dose of 8 Gray in one treatment using a single posterior-anterior beam. One group will have this treatment delivered on the MRL in a single session without the need for a prior planning CT scan, while the comparison group will follow the standard care pathway involving a planning CT appointment before radiotherapy. The study includes an optional diversity questionnaire prior to treatment and a patient experience questionnaire completed on the day of treatment. Treatment timings and patient outcomes will be monitored up to 12 months after therapy. Participants will be followed through clinical notes at 1, 3, 6, and 12 months after treatment to record their well-being and function. The study involves a recruitment period of two years with follow-up lasting one additional year. Data collected includes the timing from decision to treat to completion of therapy, patient consent times, and patient-reported experience. Participants are free to withdraw from the trial at any time without penalty.

CONDITIONS

Brief Title

To Determine Whether it is Feasible to Treat Patients Requiring Urgent Radiotherapy Diagnosed With Metastatic Cord Compression (MSCC) on the Magnetic Resonance Linear Accelerator (MRL) in a Single Appointment and Compare it to the Standard of Care Radiotherapy Pathway

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of Metastatic Spinal Cord Compression (MSCC)
  • Referred for an 8Gy single fraction radiotherapy treatment
  • 18 years or older
  • Able to give informed consent in writing or verbally
  • Willing to complete a patient experience questionnaire
  • Willing to allow the research team to review clinical notes for up to one year following treatment
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Any significant clinical disorder or laboratory finding making participation undesirable
  • Unwilling to allow researchers access to clinical notes and diagnostic scans
  • Unwilling to complete an experience questionnaire
  • Cannot speak or understand English
  • Contraindications to MRI identified after MRI safety screening
  • Unable to tolerate MRI scanning
  • Uncontrolled or poorly controlled pain
  • MSCC located in the cervical spine
  • More than one vertebral level of compression

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 1 day

Participants are screened for eligibility to participate in the trial.

1 screening visit (in-person)

Treatment

Duration - Up to 7 days from consent to treatment completion

Participants receive radiotherapy treatment for metastatic spinal cord compression either using the MR Linac in a single appointment without a prior planning CT scan or the standard pathway with a planning CT followed by radiotherapy.

1 treatment visit (in-person), plus 1 planning CT visit for standard care participants

Follow-up

Duration - 12 months

Participants complete a patient experience questionnaire on the day of treatment and clinical outcomes are monitored from clinical notes up to 12 months after treatment.

Follow-up assessments at 1, 3, 6, and 12 months post-treatment

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

C

Clinical Trial Radiographer

A

Alice Greenwood-Wilson

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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Published Research Related To This Trial

Development and psychometric testing of an instrument to measure the patient's experience of external radiotherapy: The Radiotherapy Experience Questionnaire (RTEQ).

Kristina Olausson, Annette Holst Hansson, Björn Zackrisson...

https://pubmed.ncbi.nlm.nih.gov/32095560