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A prospective,randomized,controlled clinical study of using protein hydrolysate oral solution,gastric cancer patients after surgery nitrogen balance and for intestinal stress reaction.

A prospective,randomized,controlled clinical study of using protein hydrolysate oral solution,gastric cancer patients after surgery nitrogen balance and for intestinal stress reaction.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005523
Enrollment
Unknown
Registered
2014-11-13
Start date
2014-11-20
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Gastric cancer

Interventions

Experimental group :Nutrition was infused via vein and Protein Hydrolysate Oral Solution by nasojejunal tube
Control group:Nutrition was infused via vein and physiological saline by nasojejunal tube

Sponsors

Xijing Hospital of Digestive Diseases
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Has been diagnosed with gastric cancer and receiving D2 radical treatment; 2.Age of all patients was between 40-65 years old; 3.Patients to be treated by surgery under general anesthesia; 4.Underwent open abdominal surgery; 5.Patients with preoperative NRS2002 less than 2; 6.Patients with normal liver and kidney function.

Exclusion criteria

Exclusion criteria: 1. Patients with other tumors; 2. Patients with diabetes; 3. Complete organic intestinal obstruction patients; 4. The activity of the digestive tract hemorrhage patients; 5. High flow small bowel fistula; 6. Severe enterorrhea and malabsorption; 7. Patients with severe abdominal cavity infection; 8. Patients with severe hepatic coma and azotemia; 9. Patients need preventive analgesia; 10. Pregnancy or to prepare for pregnancy or breastfeeding women; 11. Perioperative need blood plasma or blood plasma albumin; 12. Has a history of drug abuse, alcohol, or compliance is poor, can't do research according to the requirements of patients.

Design outcomes

Primary

MeasureTime frame
Laboratory examinations;

Secondary

MeasureTime frame
Peritoneal drainage tube drainage;The number of bowel sounds;Gastrointestinal initial exhaust time;Incidence of abdominal distention and diarrhea;The incidence of infection;

Countries

China

Contacts

Public ContactZhao Qingchuan
zhaoqc@fmmu.edu.cn+86 029-84771503

Outcome results

None listed

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