Clinical Trials Directory

Trials / Completed

CompletedNCT04449445

Perioperative Nutritional Optimization in Head and Neck Cancer Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
4 (actual)
Sponsor
University of Illinois at Chicago · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To determine whether nutritional optimization in head and neck cancer patients undergoing major surgery will decrease post-operative wound complications. The Investigators hypothesize that nutritional supplementation with Nestle Impact Advanced Recovery (AR) will decrease the rate of wound complications after surgery

Detailed description

The purpose of this study is to determine whether nutritional optimization in head and neck cancer patients undergoing major surgery will decrease post-operative wound complications. It is likely that many head and neck cancer patients suffer from sarcopenia, and this contributes to many wound complications, including wound infection, dehiscence, fistula formation, and free flap tissue loss. The Investigators hypothesize that nutritional supplementation with Nestle Impact Advanced Recovery (AR) will decrease the rate of wound complications after surgery

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTIsocaloric and iso-nitrogenous standard enteral tube feedsDietary supplement
DIETARY_SUPPLEMENTNestle IMPACT ARDietary supplement

Timeline

Start date
2022-05-10
Primary completion
2024-09-11
Completion
2024-09-12
First posted
2020-06-26
Last updated
2026-04-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04449445. Inclusion in this directory is not an endorsement.