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A prospective, multicenter study of the effects of preoperative oral carbohydrate (axial energy) combined with early postoperative enteral nutrition on postoperative recovery in patients with colorectal cancer

A prospective, multicenter study of the effects of preoperative oral carbohydrate (axial energy) combined with early postoperative enteral nutrition on postoperative recovery in patients with colorectal cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054459
Enrollment
Unknown
Registered
2021-12-17
Start date
2021-12-17
Completion date
Unknown
Last updated
2022-11-20

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

Conditions

Primary colorectal cancer

Interventions

Group A:Carbohydrates + early postoperative enteral nutrition
Group B:Carbohydrate
Group C:Perioperative routine management

Sponsors

People's Hospital of Deyang City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years, gender is not limited; 2. Laparoscopic colorectal cancer surgery; 3. NRS 2002>=3 points; 4. Nutritional supplementation can be carried out orally; 5. CT examination revealed no distant lymph node and blood metastases, all of which met the indications for surgery and anesthesia; 6. ASA classification I-III; 7. All selected participants agreed to participate in this study and signed.

Exclusion criteria

Exclusion criteria: 1. Those with intestinal obstruction and pyloric obstruction; 2. Reflux esophagitis, Los Angeles classification grade A and above; 3. Patients with gastroparesis; 4. Enteral EN or parenteral PN nutritional supplementation due to severe malnutrition (PG-SGA assessment of >=9 points); 5. Patients with severe underlying diseases of the heart, lung, brain and other important organs, as well as liver and kidney insufficiency, who cannot tolerate surgery; 6. Patients admitted to the ICU after surgery; 7. Has been selected for other RCT trials; 8. The patient or the legally authorized person is unwilling to participate in the trial; 9. The investigator judges that the patient is not suitable for inclusion (eg severe hypoalbuminemia; potential disputes exist).

Design outcomes

Primary

MeasureTime frame
Quality of life assessment;Nutritional risk screening (NRS-2002 scale);Human body composition analysis and determination;Time of first postoperative exhaust and defecation;Postoperative complications and length of stay;T lymphocyte subsets (CD4+, CD8+);

Countries

China

Contacts

Public ContactZhang Lili

People's Hospital of Deyang City

946930357@qq.com+86 18990204569

Outcome results

None listed

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