Clinical trial · Observational
Spectral Precise Image-Colon Cancer
CT Image Quality Assessment of Colon Cancer Using Spectral Precise Image Deep Learning Reconstruction
NCT07620444CI-TRIAL-00113263not yet recruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colon Cancer Patients | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| This is an observational study | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (2)
- measure
- subjective overall Image quality using 5-point Likert scale(1-5)
- timeFrame
- From the date of image reconstruction completion to the date of image evaluation completion, anticipated 3 Months.
- description
- Radiologist will evaluate the overall image quality using 5 Likert scale ranging from 1(poor) to 5 (Excellent)
- measure
- Objective image quality
- timeFrame
- From the date reconstruction completion to the date of image evaluation completion, anticipated 3months.
- description
- The objective image quality is evaluated by measuring the CT value shown in the image.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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.
References
Publications (0)
Data not yet available
No reference posted for this study.