Expired Study
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Madison, Wisconsin 53792


Purpose:

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%.


Criteria:

Inclusion Criteria: 1. Male or female age 18 years or older of any race-ethnicity who will undergo an elective esophagectomy or pancreaticoduodenectomy. 2. Surgery will be scheduled 5-7 days after consent date - Exclusion Criteria: 1. Surgery is urgent or emergent and/or patient would be unable to consume nutritional supplement for 5-7 days 2. Patient is currently receiving enteral (tube) or parenteral (IV) nutritional support 3. Patients with known pre-existing renal failure requiring a low protein diet 4. Patient is unable to drink 3 servings/day of a liquid supplement -


NCT ID:

NCT00585624


Primary Contact:

Principal Investigator
Kenneth A Kudsk, MD
University of Wisconsin School of Medicine & Public Health


Backup Contact:

N/A


Location Contact:

Madison, Wisconsin 53792
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 23, 2018

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