Clinical Trials in China / NCT07620444
Starting soon
Observational
Spectral Precise Image-Colon Cancer
NCT07620444 · tracked via the Priya Life Science China tracker
Condition(s) studied
Colon Cancer Patients
Investigational drug(s) / intervention(s)
This is an observational study
This is an observational study: This is an observational study
Study summary
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
Inclusion Criteria:
1. Patients pathologically confirmed with colon cancer via endoscopic biopsy.
2. Patients who underwent preoperative abdominopelvic enhanced spectral CT.
3. Study participant with age ≥ 18 years old.
4. Study participants that have signed Informed Consent Form (ICF).
Exclusion Criteria:
1. The clinical data or pathological information is considered incomplete after evaluation by the investigator.
2. The investigator determined that poor image quality (e.g. obvious artifacts, missing critical scan layers) would not satisfy post-processing analysis.
3. Data of patients deemed inappropriate for inclusion after evaluation by the investigator.
Primary outcome measure(s)
- subjective overall Image quality using 5-point Likert scale(1-5) — From the date of image reconstruction completion to the date of image evaluation completion, anticipated 3 Months.
Radiologist will evaluate the overall image quality using 5 Likert scale ranging from 1(poor) to 5 (Excellent) - Objective image quality — From the date reconstruction completion to the date of image evaluation completion, anticipated 3months.
The objective image quality is evaluated by measuring the CT value shown in the image.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Sun Yat-sen cancer center | Guangzhou | Guangdong |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07620444 on ClinicalTrials.gov ↗ ← All trials in China