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Enhancing recovery treatment of gastrointestinal function for gastrointestinal cancer patients after major abdominal surgery for gastrointestinal dysfunction, prospective impact clinical outcomes and quality of life, randomized, single-blind, controlled study

Enhancing recovery treatment of gastrointestinal function for gastrointestinal cancer patients after major abdominal surgery for gastrointestinal dysfunction, prospective impact clinical outcomes and quality of life, randomized, single-blind, controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005559
Enrollment
Unknown
Registered
2014-11-20
Start date
2014-11-30
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

Abdominal malignancies

Interventions

intervention group 1:Chewing gum (sugarless gum, 30 minutes / time, 3 times/day), to end the morning after the first eight days
intervention group 2:Incentives to patients appetite, including: patient favorite diet of media playback, 30 minutes / time, 3 times / day, around the patient can always watch their favorite fruits an
intervention group 3:6 hours after the start of oral small amount of fruit juice (orange juice, apple juice or grape juice, glucose 30g, 100ml), 12 hours after oral administration of enteral nutrition
intervention group 4:Early ambulation (day bed activities, events or bedside after a day at least 4-6 hours out of bed)

Sponsors

Second Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) The pathological diagnosis of malignant tumors elective resection patients (including cancer, bile duct cancer, pancreatic cancer, duodenal cancer, colon cancer, colorectal cancer and hepatocellular carcinoma); (2) Age: 18 years old -70 years old; (3) preoperative liver function child-pugh A grade and B grade; (4) agreed to join the study.

Exclusion criteria

Exclusion criteria: (1) there is a serious underlying disease can not tolerate surgery; (2) there is a history of abdominal surgery, abdominal adhesions and release time greater than 30 minutes; (3) is currently undergoing hormone therapy; (4) lactating women; (5) hypersensitivity to any component EN.

Design outcomes

Primary

MeasureTime frame
Alanine aminotransferase;Alkaline phosphatase;Total bilirubin;Prealbumin;Prothrombin time;Platelet count;C-reactive protein;Peripheral endotoxin;Ventilation time;Defecation;Up to 2/3 of the required amount of time for oral consumption;Hospital stay;Hospital costs;The complication rate;Quality of Life;

Countries

China

Contacts

Public ContactXu Pengyuan
pyxu778@sina.com+86 13013331809

Outcome results

None listed

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