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Clinical Trials/NCT05380609
NCT05380609
Enrolling By Invitation
Not Applicable

Accelerated Body Diffusion-Weighted MRI Using Artificial Intelligence

Royal Marsden NHS Foundation Trust1 site in 1 country450 target enrollmentMay 6, 2022
ConditionsCancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cancer
Sponsor
Royal Marsden NHS Foundation Trust
Enrollment
450
Locations
1
Primary Endpoint
Qualitative image comparison
Status
Enrolling By Invitation
Last Updated
3 years ago

Overview

Brief Summary

Whole-body diffusion-weighted MRI (WBDWI) is a non-invasive tool used for staging and response evaluation in oncologic practice and is at the core of emerging response criteria in advanced prostate and breast cancers.

WBDWI is a sensitive tool that radiologists can use to review the extent of disease and is achieved using a series of sequential imaging stations from the head to the mid-thigh. WBDWI accounts for more than 50% of the acquisition time of conventional whole-body MRI studies with a 1-hour duration. Despite national and international guidance for using whole-body MRI, a recent UK survey indicated that only 27% of UK radiology departments were offering a whole-body MRI service with a lack of scanner availability cited by 50% of respondents as the main challenge to service delivery. In the context of the ever-increasing capacity pressures on MRI departments, reducing acquisition times would facilitate the wider adoption of clinical WBDWI, reduce costs, and improve the patient experience.

DWI is also embedded into consensus MRI protocols across almost all tumour types including primary prostate and breast cancers, metastatic liver disease, gynaecological cancers & GI cancers, where acquisition time savings could also be beneficial. The investigators have previously published accelerated DWI with deep learning based denoising filters (quickDWI), which can provide up to 50% reduction in whole-body MRI acquisition times. The goal of the deep-learning algorithm is to remove the noise in these subsampled images, producing an image with acceptable clinical quality.

The aim of this investigation is to extend this work by testing quickDWI within a larger retrospective data cohort, incorporating other cancers such as disease of the abdomen and pelvis, primary prostate cancer, liver metastases, and pancreatic cancer.

Registry
clinicaltrials.gov
Start Date
May 6, 2022
End Date
April 2025
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • No exclusion criteria as this is a retrospective data study only.

Outcomes

Primary Outcomes

Qualitative image comparison

Time Frame: Throughout study completion, 3 years

The primary endpoint is the qualitative comparison of radiological image quality on a 5-point Likert scale (5 being the best) for quickDWI images and conventional clinical images.

Secondary Outcomes

  • Qualitative contrast-to-noise-ratio comparison(Throughout study completion, 3 years)
  • Repeatability comparison(Throughout study completion, 3 years)
  • Qualitative artefact comparison(Throughout study completion, 3 years)
  • Inter-observer comparison(Throughout study completion, 3 years)

Study Sites (1)

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