Evaluation of an Artificial Intelligence Algorithm Reducing Noise on Fast Whole-body Bone Tomoscintigraphy Acquisitions Recorded by a 360 Degree Cadmium-Zinc-Tellurid Camera (IATOS2)

February 28, 2025 updated by: Achraf BAHLOUL, Central Hospital, Nancy, France

Recently, artificial intelligence algorithms reducing noise by deep learning have been developed with application to SPECT and PET images.

Many studies have reported the possibility of reducing the recording time in bone scintigraphy by applying artificial intelligence algorithms reducing noise

Study Overview

Status

Recruiting

Conditions

Detailed Description

Only two studies compared images denoised by a Deep Learning algorithm to those denoised by conventional filters (Gaussian and median filters). The first study was conducted only on patients, without phantom analysis and without taking into account the size of the lesions. The second study included an analysis on phantom and patients, but with application to planar images rather than to SPECT images that are increasingly used today

The hypothesis of our study conducted on phantom and patients is that an artificial intelligence algorithm reducing noise could replace the conventional filters usually used in bone SPECT for the denoising of scintigraphic images.

Study Type

Observational

Enrollment (Estimated)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Vandoeuvre les Nancy cedex, France, 54511
        • Recruiting
        • Nuclear Medicine Department
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Patients who had a whole-body thee dimensions bone scan for rheumatological or oncological indications and non opposed to th use of their data

Description

Inclusion Criteria:

Patients who had a whole-body thee dimensions bone scan for rheumatological or oncological indications.

Exclusion Criteria:

Patients opposed to the use of their data

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To compare imaging treated by the intelligence artificial algorithm with imaging treated with the traditionnal filter artificial algorithm
Time Frame: one day
Quantification value on imaging measured with intelligence artificial algorithm compared with quantification value measured with conventional filter
one day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 27, 2025

Primary Completion (Estimated)

March 15, 2025

Study Completion (Estimated)

March 30, 2025

Study Registration Dates

First Submitted

January 7, 2025

First Submitted That Met QC Criteria

January 14, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 28, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • 2024PI241

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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