Preoperative Nutritional Support in Esophagectomy or Pancreaticoduodenectomy
Completed · Not applicable
Conditions studied: Esophagectomy, Pancreaticoduodenectomy
In brief
We are proposing to evaluate the benefit of preoperative nutritional support with Impact Advanced Recovery in the most vulnerable group of elective gastrointestinal surgery patients who may experience a complication, esophagus and pancreas resections, and hypothesize that oral supplementation with 3 servings (0.75 L) Impact Advanced Recovery will reduce postoperative stay by 10-20% and reduce the incidence of major complications by 25%.
Key facts
- Study ID
- NCT00585624
- Run by
- University of Wisconsin, Madison
- People needed
- 344
- Starts
- 2007-04-01
- Expected to finish
- 2009-10-01
- Last updated by the study team
- 2015-10-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female age 18 years or older of any race-ethnicity who will undergo an elective esophagectomy or pancreaticoduodenectomy.
- Surgery will be scheduled 5-7 days after consent date -
You may not qualify if…
- Surgery is urgent or emergent and/or patient would be unable to consume nutritional supplement for 5-7 days
- Patient is currently receiving enteral (tube) or parenteral (IV) nutritional support
- Patients with known pre-existing renal failure requiring a low protein diet
- Patient is unable to drink 3 servings/day of a liquid supplement -
Where it is running
- University of Wisconsin Hospital & Clinics — Madison, Wisconsin, United States
Full record on ClinicalTrials.gov
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