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MR Guidance for Liver and Pancreas

Recruiting
Conditions
Magnetic Resonance Imaging
Interventions
Other: MRI
Registration Number
NCT03582189
Lead Sponsor
University Health Network, Toronto
Brief Summary

This is a single centre, single arm, prospective feasibility study that aims to see whether magnetic resonance imaging (MRI) as a source of image guidance before each radiation treatment fraction is feasible, and also if it may provide information that could potentially be used during the treatment to improve the radiation treatment plan.

Patients will have 5 MRIs with each of their RT sessions. If patients' RT treatment will consist of more than 5 fractions, only 5 MRIs will be done with any 5 RT fractions. Patients will be completing a short questionnaire at the end of each MRI. A patient questionnaire will also be completed at the end of the study to assess for patient satisfaction.

There will be 30 evaluable patients enrolled to the study.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Patients 18 years or older
  • Diagnosed with locally advanced pancreatic cancer or hepatocellular carcinoma being considered for treatment with chemoradiation, long course RT, or SBRT with curative intent or palliative intent, planned for 5 or more RT fractions
Exclusion Criteria
  • Contraindications for MRI: ferromagnetic prosthesis, pacemaker / implanted defibrillator, claustrophobia

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Liver MetastasesMRIApproximately 10 patients with liver mets will be enrolled to the study with the primary aim of determining the feasibility of using off-line MRI-guidance during the course of radiation treatment
Pancreatic CancerMRIApproximately 10 patients with pancreatic cancer will be enrolled to the study with the primary aim of determining the feasibility of using off-line MRI-guidance during the course of radiation treatment
Hepatocellular carcinomaMRIApproximately 10 patients with HCC will be enrolled to the study with the primary aim of determining the feasibility of using off-line MRI-guidance during the course of radiation treatment
Primary Outcome Measures
NameTimeMethod
Patient Satisfaction SurveyAt study completion (day5 or week 5, depending on type of treatment)

To evaluate patient satisfaction with the MR guidance process, a modified version of a questionnaire previously used at our institution will be performed at the end of the study

MRI-Anxiety QuestionnairePrior to or before MR session 5 (day 5 or week 5, depending on type of treatment)

his instrument will be used to evaluate patient related anxiety after each MR

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University Health Network - Princess Margaret Cancer Centre

🇨🇦

Toronto, Ontario, Canada

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