Obstructive Colorectal Cancer
Conditions
Interventions
Experimental Group:Following placement of the intestinal decompression tube, patients in the intervention group received trophic oral nutritional supplementation (ONS) for a minimum of 5 days. The tro
Control Group:Patients in the control group were kept nil per os (NPO) and received total parenteral nutrition (TPN) at 25 kcal/kg/day. Standard supportive care was provided, including gastric acid su
Sponsors
The Second Affiliated Hospital of Kunming Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 90 Years
Inclusion criteria
Inclusion criteria: 1.Aged 18 years or older. 2. Patients diagnosed with colorectal cancer accompanied by incomplete intestinal obstruction via abdominal X-ray and abdominal CT examination, who had undergone placement of a transnasal intestinal decompression tube; the tube tip was confirmed to have reached the terminal ileum by abdominal upright radiography, with no significant air-fluid levels observed in the proximal bowel, followed by elective radical resection. 3. Voluntarily participated in the study and provided written informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients requiring emergency surgery, including but not limited to acute complete intestinal obstruction, bowel perforation, severe peritonitis, or sepsis secondary to colon cancer with obstruction necessitating immediate surgical intervention. 2.Pregnant or lactating women. 3.Patients on long-term high-dose corticosteroid therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of Infectious Complications;Intestinal Barrier Function;Postoperative Length of Hospital Stay; | — |
Secondary
| Measure | Time frame |
|---|---|
| Serum Intestinal Barrier Markers; | — |
Countries
China
Contacts
Public ContactSun Dali
The Second Affiliated Hospital of Kunming Medical University
Outcome results
None listed