Defining Dosimetric Reference Levels in Computed Tomography Spectral Scanning

NCT07305103 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 9600

Last updated 2025-12-26

No results posted yet for this study

Summary

Spectral computed tomography or dual-energy CT imaging can overcome the limitations of conventional CT in differentiating between two materials with equivalent total attenuation. It can generate several types of images, such as virtual monochromatic images, which improve the contrast-to-noise ratio for low energy levels and reduce artifacts for high energy levels. It also allows for quantitative image analysis and thus better characterization of lesions and tissues through material mapping (e.g., iodinated contrast agent mapping). This technique is increasingly used in routine clinical practice thanks to improvements in image flow management and technological advances. It also involves exposing patients to ionizing radiation, as with conventional CT but, unlike conventional CT scans, for which dosimetric reference levels (RLs) are defined for the most common examinations in France (RL decree dated 2019), there are currently no dosimetric reference levels for examinations performed using this technique. Yet RLs are an important and effective tools for optimizing patient exposure to ionizing radiation. Several articles were published between 2012 and 2017 when the first dual-energy scanners arrived in clinics. However, the results presented in these studies are now far removed from recent practices, as they do not take into account the latest technological developments used in dual-energy scanners, which reduce X-ray doses.

The main objective of the study is to define dosimetric reference levels for the most commonly performed spectral computed tomography examinations in France.

Conditions

  • Medical Imaging

Interventions

RADIATION

Spectral ComputedTomography

Commonly performed spectral computed tomography examinations in France

Sponsors & Collaborators

  • Institut Paoli Calmettes, Marseille

    collaborator UNKNOWN
  • Hôpital Necker-Enfants Malades

    collaborator OTHER
  • Lille University Hospital

    collaborator UNKNOWN
  • CHU Hôpital Lariboisière APHP

    collaborator UNKNOWN
  • Centre Hospitalier Universitaire de Saint Etienne

    collaborator OTHER
  • Saint-Louis Hospital, Paris, France

    collaborator OTHER
  • Bichat Hospital, Paris, France

    collaborator UNKNOWN
  • Hôpital Louis Mourier, 92700 Colombes

    collaborator UNKNOWN
  • Centre Hospitalier de Valenciennes

    collaborator NETWORK
  • Hopital Louis Pradel

    collaborator OTHER
  • Centre Léon Bérard, Lyon

    collaborator UNKNOWN
  • University Hospital, Bordeaux

    collaborator OTHER
  • Centre Hospitalier Lyon Sud

    collaborator OTHER
  • Institut Curie

    collaborator OTHER
  • Amiens University Hospital

    collaborator OTHER
  • Poitiers University Hospital

    collaborator OTHER
  • Henri Mondor Hospital, Créteil

    collaborator UNKNOWN
  • Saint Antoine University Hospital

    collaborator OTHER
  • Nord Ardennes Intercommunal Hospital

    collaborator UNKNOWN
  • Centre Antoine Lacassagne, Nice

    collaborator UNKNOWN
  • Hôpital Edouard Herriot (GH Centre), Lyon

    collaborator UNKNOWN
  • Centre Hospitalier Universitaire de Nīmes

    lead OTHER

Principal Investigators

  • Joël GREFFIER · Nîmes University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-01
Primary Completion
2025-12-31
Completion
2026-06-30

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07305103 on ClinicalTrials.gov