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Prospective Evaluation and Individualized Prediction Model for Multidimensional Risks in Postoperative Patients with Colorectal Cancer and Liver Cirrhosis

Prospective Evaluation and Individualized Prediction Model for Multidimensional Risks in Postoperative Patients with Colorectal Cancer and Liver Cirrhosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127833
Enrollment
Unknown
Registered
2026-07-08
Start date
2026-07-08
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal cancer combined with liver cirrhosis

Interventions

control group:None

Sponsors

Mengchao Hepatobilary Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with liver cirrhosis based on imaging, laboratory tests, and clinical history ; 2. Patients with newly diagnosed primary CRC confirmed by pathology and assessed tumor staging as stage I-III (i.e. no distant metastasis) ; 3. Intending to undergo elective radical surgery for colorectal cancer with informed consent from the patient/legal representative.

Exclusion criteria

Exclusion criteria: 1. Emergency surgery patients (e.g., requiring urgent surgery due to intestinal obstruction, perforation, massive bleeding, etc.); 2. Patients with severe dysfunction of other vital organs (e.g., severe cardiac insufficiency (NYHA class III-IV), chronic kidney disease stage IV-V, etc.); 3. Patients with other uncontrolled malignant tumors; 4. History of major abdominal surgery; 5. Unstable state of decompensated cirrhosis (e.g., acute variceal bleeding within 4 weeks before surgery, acute hepatic encephalopathy (grade 2 or above), acute bacterial peritonitis, etc.); 6. Patients suspected of hereditary colorectal cancer; 7. Patients unable to cooperate with the study or follow-up;

Design outcomes

Primary

MeasureTime frame
Incidence of severe postoperative complications within 30 days (Clavien-Dindo grade =3);

Secondary

MeasureTime frame
Secondary clinical endpoints within 30 days postoperatively (reoperation rate, readmission rate, mortality, length of hospital stay, ICU admission rate and duration, total medical costs within 30 days;Liver reserve function related indicators (Child Pugh, MELD, etc.);Peripheral blood biomarkers of inflammation, immunity and liver fibrosis;

Countries

China

Contacts

Public ContactLin Suyong

Mengchao Hepatobilary Hospital of Fujian Medical University

lsy02090@126.com+86 591 88112802

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026