NCT06024837

Brief 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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2023

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 7, 2023

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

August 21, 2023

Completed
16 days until next milestone

First Posted

Study publicly available on registry

September 6, 2023

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2025

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2025

Completed
Last Updated

September 20, 2024

Status Verified

September 1, 2024

Enrollment Period

1.6 years

First QC Date

August 21, 2023

Last Update Submit

September 19, 2024

Conditions

Keywords

Colo-rectal cancerspectral CT scanliver metastasesperitoneal carcinosis

Outcome Measures

Primary Outcomes (2)

  • 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

  • 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 Outcomes (2)

  • Evaluation of response to chemotherapy in RECIST 1.1

    Year : 1

  • Evaluation of response to chemotherapy in Radiomics

    Year : 1

Study Arms (1)

Patients with Colo-rectal Cancer

Patients with Colo-rectal Cancer will be included.

Other: CT Images

Interventions

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

Patients with Colo-rectal Cancer

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with synchronous or metachronous peritoneal and/or liver metastases of colorectal cancer with curative surgical plans.

You may qualify if:

  • Patients followed for colorectal cancer with synchronous or metachronous liver metastases and/or peritoneal carcinosis
  • Patients with a curative surgical resection plan

You may not qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Saint-Etienne

Saint-Etienne, 42000, France

RECRUITING

MeSH Terms

Conditions

Colonic Neoplasms

Condition Hierarchy (Ancestors)

Colorectal NeoplasmsIntestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal Diseases

Study Officials

  • Rémi GRANGE, MD

    CHU SAINT-ETIENNE

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 21, 2023

First Posted

September 6, 2023

Study Start

June 7, 2023

Primary Completion

January 1, 2025

Study Completion

June 1, 2025

Last Updated

September 20, 2024

Record last verified: 2024-09

Data Sharing

IPD Sharing
Will not share

Locations