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Clinical Trials/NCT00539097
NCT00539097
Terminated
Phase 2

Evaluation Perioperative Nutrition on Donor Site Healing in Patients Undergoing Reconstructive Burn Surg

Shriners Hospitals for Children1 site in 1 country38 target enrollmentJune 2005
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ConditionsBurnReconstructive Surgical Procedure

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Burn
Sponsor
Shriners Hospitals for Children
Enrollment
38
Locations
1
Primary Endpoint
donor site healing time
Status
Terminated
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The investigators hope to learn if taking a nutrition drink for a short time after surgery for an elective reconstructive burn injury improves donor site healing, muscle mass and scar maturation time (the point at which the redness, height and firmness of the wound has faded, flattened and softened, and no longer changes in appearance).

Registry
clinicaltrials.gov
Start Date
June 2005
End Date
October 2007
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Theresa Mayes

Clinical Dietitian

Shriners Hospitals for Children

Eligibility Criteria

Inclusion Criteria

  • •At least one year post-acute burn injury
  • •Admitted for surgery whereby split thickness donor site created
  • •Received initial acute treatment at Shriner's Hospital in Cincinnati

Exclusion Criteria

  • •Less than 6years of age
  • •Less than one year from acute burn injury
  • •Split thickness donor site/autograft not anticipated
  • •Initial treatment not at Shriners Hospital in Cincinnati

Outcomes

Primary Outcomes

donor site healing time

Time Frame: 3weeks

Study Sites (1)

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