Postoperative Oral Intake Trial
Study Details
Study Description
Brief Summary
Complete fasting until resumed bowel function after upper abdominal surgery is not beneficial. Enteral feeding has been claimed to be the preferred way of delivering nutritional support postoperatively. Increasing evidence suggests that letting patients eat ("voluntary oral feeding" or "oral intake at will") from the day after the operation is safe. No prospective randomised trial has been undertaken to compare these two regimens. In this study, the investigators will randomise 444 patients, subject to major upper abdominal surgery, into receiving either continuous enteral feeding by needle catheter jejunostomy until resumed bowel function, or to oral intake at will from postoperative day 1. The main endpoints are the incidence rate of major complications and death, as well as a Quality of Life assessment.
Null-Hypothesis:
Routine postoperative feeding by needle catheter jejunostomy after major, upper abdominal surgery has no clinically relevant advantages over early oral intake at will.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1 |
Detailed Description
Complete fasting until resumed bowel function after upper abdominal surgery is not beneficial. Enteral feeding has been claimed to be the preferred way of delivering nutritional support postoperatively. Increasing evidence suggests that letting patients eat ("voluntary oral feeding" or "oral intake at will") from the day after the operation is safe. No prospective randomised trial has been undertaken to compare these two regimens. In this study, we will randomise 444 patients, subject to major upper abdominal surgery, into receiving either continuous enteral feeding by needle catheter jejunostomy until resumed bowel function, or to oral intake at will from postoperative day 1. The main endpoints are the incidence rate of major complications and death, as well as a Quality of Life assessment.
Null-Hypothesis:
Routine postoperative feeding by needle catheter jejunostomy after major, upper abdominal surgery has no clinically relevant advantages over early oral intake at will.
Study Design
Outcome Measures
Primary Outcome Measures
- Major complications within 8 weeks postoperatively []
Secondary Outcome Measures
- Minor complications []
- Quality of Life []
- Use of analgesics []
- Post-laparotomy bowel movement []
Eligibility Criteria
Criteria
Inclusion Criteria:
- Adults subject to major, upper, open abdominal surgery (exceeding simple cholecystectomies and fundoplications)
Exclusion Criteria:
-
Crohns disease
-
Mentally disabled
-
Pre-op dependency on intravenous (IV) nutrition
-
Expected life duration of less than 3 months
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University Hospital Northern Norway, | Tromsø, | Tromsø | Norway | 9038 |
Sponsors and Collaborators
- University Hospital of North Norway
Investigators
- Study Chair: Arthur Revhaug, Professor, University of Northern Norway
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- NFR 147339/320