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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06024837
Other study ID # IRBN1162022/CHUSTE
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 7, 2023
Est. completion date June 2025

Study information

Verified date August 2023
Source Centre Hospitalier Universitaire de Saint Etienne
Contact Rémi GRANGE, MD
Phone (0)477828963
Email remi.grange@chu-st-etienne.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Spectral CT is a rapidly expanding imaging modality that allows a reduction in iodine dose and irradiation compared to conventional scanning. It uses the difference in attenuation of the material according to the two different energy levels of the incident x-ray beams. The dual-energy scanner has a wide range of clinical applications, particularly in abdominal imaging.


Description:

First of all, the virtual creation of mono-energy images between 40 and 140 keV has shown subjective and objective improvement of tumor detection of hypovascular lesions using low energies (40keV). It has been shown to be of interest in vascular and cardiac imaging, and to reduce artefacts in bone imaging. However, its performance in oncology analysis has been little studied. The selection of patients for peritoneal and hepatic carcinosis surgery is fundamental, as surgery allows a prolongation of survival, but are associated with a non-negligible morbi-mortality rate. Spectral CT provides improved detection of peritoneal carcinosis and liver metastases of colorectal cancer compared to conventional CT acquisition.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date June 2025
Est. primary completion date January 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Patients followed for colorectal cancer with synchronous or metachronous liver metastases and/or peritoneal carcinosis - Patients with a curative surgical resection plan Exclusion Criteria: - Patients with non-metastatic colorectal cancer - Patients treated with chemotherapy without surgical plans - Patients with colorectal cancer with extra-hepatic and extra-peritoneal metastases alone (e.g. lung, bone)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
CT Images
Analysis of CT images of peritoneal and/or liver metastases from colorectal cancer

Locations

Country Name City State
France CHU Saint-Etienne Saint-Étienne

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of peritoneal lesion mapping between spectral scanning and conventional scanning Comparison of peritoneal lesion mapping between spectral scanning (monoenergetic acquisitions, iodine mapping, etc.) and conventional scanning (acquisition obtained during spectral acquisition). Year : 1
Primary Comparison of hepatic lesion mapping between spectral scanning and conventional scanning Comparison of hepatic lesion mapping between spectral scanning (monoenergetic acquisitions, iodine mapping, etc.) and conventional scanning (acquisition obtained during spectral acquisition). Year : 1
Secondary Evaluation of response to chemotherapy in RECIST 1.1 Collection of demographic, biological and surgical data. Year : 1
Secondary Evaluation of response to chemotherapy in Radiomics Collection of demographic, biological and surgical data. Year : 1
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