CClinicalTrials.gg
Enrolling by invitationNCT05380609CeleScan-RUpdated May 19, 2022

Accelerated Body Diffusion-Weighted MRI Using Artificial Intelligence

An observational study in Cancer, sponsored by Royal Marsden NHS Foundation Trust. Enrolling by invitation at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-05-19.

Sponsored by Royal Marsden NHS Foundation Trust · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2025, 1 year 6 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
450
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Cancer

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03

In context

Body Weight

1,223 studies on the registry are indexed under Body Weight; 131 are open to participants now.

This study's planned enrollment of 450 is above the median of 140 across 238 observational studies indexed under Body Weight.

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Lead sponsor

Royal Marsden NHS Foundation Trust is the lead sponsor of 262 studies on the registry; 49 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Cancer patients

Eligibility criteria

  1. Patients who have received one of the following MRI examinations (scan type shown in parentheses):

    • Multiple Myeloma (whole-body)
    • Metastatic Prostate Cancer (whole-body)
    • Metastatic Breast Cancer (whole-body)
    • Liver Metastases (stacked abdomen/pelvis)
    • Pancreatic Cancer (stacked abdomen/pelvis)
    • Gynaecological Cancers (stacked abdomen/pelvis)
    • Gastrointestinal Cancers (stacked abdomen/pelvis)
    • Primary Prostate Cancers (multiparametric Prostate exam)
  2. Patients who have received one of the above-mentioned scan types using a modified clinical multi-direction diffusion-weighted (MDDW) MRI protocol as part of standard of care.

Exclusion Criteria:

  • No exclusion criteria as this is a retrospective data study only.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
450 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Qualitative image comparison

    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.

    Time frame: Throughout study completion, 3 years

Secondary outcomes

  1. Qualitative contrast-to-noise-ratio comparison

    Qualitative radiological contrast-to-noise-ratio (CNR) on a 5-point Likert scale (5 being the best), for quickDWI images and conventional clinical images.

    Time frame: Throughout study completion, 3 years

  2. Qualitative artefact comparison

    Qualitative scoring for presence of image artefacts on a 5-point Likert scale (5 being the best), for quickDWI images and conventional clinical images.

    Time frame: Throughout study completion, 3 years

  3. Inter-observer comparison

    Krippendorff's alpha coefficient for inter-observer agreement of image quality, CNR and image artefacts.

    Time frame: Throughout study completion, 3 years

  4. Repeatability comparison

    The coefficient of repeatability of median ADC measurements within regions-of-interest (ROIs) defined in the same anatomical areas on both quickDWI and standard clinical imaging.

    Time frame: Throughout study completion, 3 years

07

Study locations

1 site
  • Department of Radiology, The Royal Marsden NHS Foundation Trust
    Sutton, Surrey SM2 5PT, United Kingdom
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 19, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05380609
Lead sponsor
Royal Marsden NHS Foundation Trust
Responsible party
Sponsor
First posted
May 19, 2022
Start date
May 6, 2022
Primary completion
Apr 2025 (estimated)
Completion
Apr 2025 (estimated)
Last update
May 19, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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