Clinical trial · Observational
Development of a Set of Auxiliary Decision-making System for the Perioperative Period of Hepatectomy Based on Static CT and Artificial Intelligence.
NCT07056270CI-TRIAL-00091897not 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)
The study will prospectively recruit patients with chronic liver disease and liver cancer for static CT scans to establish a high-definition CT database. Combining clinical data and pathological information, artificial intelligence technology will be utilized to construct models for assessing liver function and liver cirrhosis, as well as predicting microvascular invasion (MVI).
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Liver Cancer | Malignant Liver Neoplasm | CURATED_EXACT | 0.92 |
| Liver Cirrhosis | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| static CT scans | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Static CT group
- description
- Patients with chronic liver disease and liver cancer receive static CT scans
- interventionNames
- Other: static CT scans
Primary outcomes (3)
- measure
- microvascular invasion
- timeFrame
- 7 days after surgery
- description
- microvascular invasion based on pathology
- measure
- liver cirhosis
- timeFrame
- 7 days after surgery
- description
- liver cirhosis according to laennec grading system
- measure
- liver function
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients who are clinically diagnosed with primary liver cancer and other space-occupying liver lesions preoperatively and are planned for surgical resection, or those with underlying liver diseases and cirrhosis; 2. Aged 18-75 years; 3. Willing to participate in this study and have signed the informed consent. Exclusion Criteria: 1. Planned or unplanned pregnancy and pregnant women; 2. Glomerular filtration rate (GFR) ≤60 ml/min; 3. History of contrast media allergy.
References
Publications (0)
Data not yet available
No reference posted for this study.