About this trial
This is a single-center, comparative, observational study. Datasets will be collected from patients with pathologically confirmed colon cancer who undergo abdomen-pelvis enhanced spectral CT scan.
Eligibility criteria
Qualifiers
Patients pathologically confirmed with colon cancer via endoscopic biopsy.
Patients who underwent preoperative abdominopelvic enhanced spectral CT.
Study participant with age ≥ 18 years old.
Study participants that have signed Informed Consent Form (ICF).
Disqualifiers
The clinical data or pathological information is considered incomplete after evaluation by the investigator.
The investigator determined that poor image quality (e.g. obvious artifacts, missing critical scan layers) would not satisfy post-processing analysis.
Data of patients deemed inappropriate for inclusion after evaluation by the investigator.
Trial design
Treatments tested in this trial
- This is an observational study
Treatment groups
Sponsors and collaborators
Philips Clinical & Medical Affairs Global
Lead sponsor
Sun Yat-Sen University Cancer Center
Collaborator