RecruitingNot ApplicableNCT05823272

ONS in Gastric Cancer After Total Gastrectomy

Effect of Oral Nutritional Supplement on Nutritional Status and Clinical Outcome in Gastric Cancer Patients After Total Gastrectomy


Sponsor

Jinling Hospital, China

Enrollment

60 participants

Start Date

Mar 22, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Gastric cancer patients after total gastrectomy will be randomized to oral nutritional supplement group or control group at discharge. Patients will receive 6 months of oral nutritional supplement or normal diet after discharge. The primary and secondary outcomes will be collected.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria5

  • Informed consent of patients or their legal representatives to participate in this study
  • consecutive adult (18-80 years) patients underwent radical gastrectomy (total gastrectomy)
  • nutrition Risk Screening (NRS) 2002≥3 at discharge
  • eastern Cooperative Oncology Group (ECOG) score of 0-2 at discharge
  • normal liver and kidney function

Exclusion Criteria9

  • unable to oral or consume ONS
  • allergy to any ingredient in the oral nutrition powder
  • pregnancy
  • palliative surgery or gastric stump cancer
  • congenital acquired immune deficiency disease
  • severe liver and kidney diseases including active hepatitis, cirrhosis, and uremia diabetes has developed complications or uncontrolled by medications
  • motor system diseases cannot complete grip strength measurement and 5-time chair stand test
  • have cognitive impairment, unable to complete the relevant questionnaires
  • expected to require tube feeding after discharge from the hospital

Interventions

OTHERONS

oral nutritional supplement


Locations(1)

Jinling Hospital, China

Nanjing, Jiangsu, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05823272


Related Trials