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NCT Number: NCT06440616

Benefit of Spectral Information in Patients Suspected for Lung Cancer

Purpose The aim of the study is to investigate the utilization of photon counting CT (PCCT) and the spectral information provided to determine the impact of spectral information on follow-up examinations.

As secondary aims we will compare conventional CT, CT + 18Flouro-deoxy-glucose (18F-FDG) positron emission tomography (PET) and PCCT + 18F-FDG PET for the tumor-node-metastasis (TNM) staging of lung cancer patients.

PCCT with and without spectral information to assess the need for additional work-up,TNM classification, and sensitivity/specificity for malignant lesions. Patients will be randomized for reading with or without spectral information available within a clinical setting. The clinical readings are performed as a structured reports of all significant findings. Including both malignant and benign findings. Furthermore, in case additional follow-up/work-up is needed based on the guidelines on incidental findings by the American College of Radiology (ACR), this will be reported as well. If lesions suspicious of pulmonary malignancy is present, a provisional TNM classification is provided based on the scan findings.

After 3 months, the patient record is reviewed where additional examinations that can be attributed to the PCCT scan are recorded. The financial impact is calculated by a health economist based on the findings. PET/CT, conventional CT and PCCT combined with PET will be assessed retrospectively for comparison. Endpoints are number of supplementary examinations and cost savings. Sensitivity and specificity for any malignant finding. The T, N and M stages are assessed separately as diagnostic measures by the McNemar's test with a reference standard from the Danish Lung cancer register. The number of malignant lesions will be determined by reviewing the patient records incl. pathology assessment if available 12 months after inclusion of the last patient.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Copenhagen University Hospital Herlev

Herlev, Capital Region, 2730, Denmark

Location status: Recruiting

Location contact

Michael B Andersen, PhD

CONTACT

[email protected]

38 68 38 68 ext. +45

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients suspected of lung cancer refered to Copenhagen University Hospital as per the guidelines from the danish national health authorities from either the general practitioner or from the department of pulmonology.
  • Informed consent

Exclusion criteria

  • Patients who cannot tolerate intravenous iodinated contrast
  • Already verified lung cancer from another institution
  • Comorbidities that exclude the patient from receiving treatment
  • Lack of reference standard in the form of either histology or follow-up
  • Known extrapulmonary malignancy
  • Technical limitations within the scans/reconstructions
  • other

Pr. the 29th of September included 433 participants.

Treatment and study plan

Spectral CT images generated by a photon counting CT scanner

Device

The reading radiologist will in the experimental arm have access to spectral CT images in the form of low virtual monoenergetic images, virtual non-contrast images, iodine maps and effective atomic number. In the non-interventional arms the reading radiologist will only have access to conventional CT images.

Primary outcomes

  1. Number of follow up examinations

    Time frame: Baseline

    Determine the number of suggested follow-up examinations based on the initial CT scan to learn the significance of spectral information in a clinical setting.

Secondary outcomes

  1. T, N, and M stage

    Time frame: 24 months

    Determine the accuracy of T, N, and M stage based on PCCT, conventional CT, PET/CT and PET/PCCT. Retrospective assessment 24 months after primary scan.

  2. Number of malignant lesions

    Time frame: 24 months

    Determine the number of found malignant lesions in each arm. Reference standard will be follow up or pathology within a minimum of one year of the scan. That means 12 months after the end of the inclusion period.

Study contacts

Contact information is provided by the study sponsor or research team.

Michael B Andersen, PhD

CONTACT

[email protected]

38 68 38 68 ext. +45

Sponsors and collaborators

Lead sponsor

Copenhagen University Hospital at Herlev

Other

Collaborators

  • Aarhus University Hospital
  • Rigshospitalet, Denmark

Registry information

Official study title

Benefit of Spectral Information Provided by Photon Counting CT in Patients Suspected for Lung Cancer

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Jun 4, 2024
Registry last updated
Mar 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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