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Effects of immune-enhanced enteral nutrition on immune and nutritional status in patients with advanced colon tumors

Effects of immune-enhanced enteral nutrition on immune and nutritional status in patients with advanced colon tumors

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072904
Enrollment
Unknown
Registered
2023-06-27
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Colon cancer

Interventions

Immune-fortified group:Oral administration of "suyisu" 400ml per day
Standard nutrition group:Oral administration of "jialichang" 400ml per day
negative control group:Dietary guidance

Sponsors

Changzhou NO.2 People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) It meets the diagnostic criteria for colon cancer in the 2017 Chinese Society of Clinical Oncology (CSCO) guidelines, and is diagnosed by computed tomography (CT) and colonoscopy before surgery, and confirmed by pathological examination after colon cancer after surgery. (2) Patients who have developed distant metastasis or lymph node metastasis, diagnosed with advanced colon cancer, and need to receive at least four cycles of chemotherapy were included in the study. (3) After nutritional risk screening and nutritional assessment, patients with NRS 2002=3 score and PG-SGA score of =4 were included in the study. (4) Karnofsky Functional Status Score (KPS Score) > 50 points. (5) Age= 40 years old, = 80 years old. (6) Life expectancy is at least 6 months.

Exclusion criteria

Exclusion criteria: Gastrointestinal obstruction; Perforation or bleeding of the digestive tract; severe hepatic insufficiency (serum aminotransferases greater than five times normal); severe renal insufficiency (CKD stage 4 and above); severe cardiac insufficiency (NYHA grade 4); severe myelosuppression (myelosuppression grade IV) and/or other conditions deemed clinically unsuitable for inclusion; are receiving thrombolytic or anticoagulant therapy; Allergy to study drugs.

Design outcomes

Primary

MeasureTime frame
Plasma albumin;immunoglobulin;

Secondary

MeasureTime frame
quality of life;

Countries

china

Contacts

Public ContactShi Li

Changzhou NO.2 People's Hospital

shili1204@sina.com+86 138 6119 3196

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026