Clinical Trials Directory

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RecruitingNCT01731444

Phenylephrine Tumescence for Hemostasis in Surgery for Burn Injury

Phenylephrine Tumescence for Hemostasis in Surgery for Burn Injury - A Randomized Control Trial

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
University of Manitoba · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The standard of care for treatment of burn injury is to inject a solution of epinephrine under the skin of the injured site in order to reduce blood loss during skin grafting. This solution of epinephrine has been shown to have effects on the body outside the donor site. Some people have increases in heart rate and blood pressure. We will study the effect of a phenylephrine solution in place of an epinephrine solution to control blood loss. We think that phenylephrine will help decrease blood loss and not change blood pressure or heart rate. The injured area will be injected under the skin and a skin graft will be taken in the same way as we usually do. The only change will be the use of phenylephrine in the solution instead of epinephrine. Our goal is to find whether or not phenylephrine or epinephrine solution results in a reduction of blood loss without affecting the rest of the body.

Conditions

Interventions

TypeNameDescription
DRUGPhenylephrine

Timeline

Start date
2014-12-01
Primary completion
2026-06-01
Completion
2027-12-01
First posted
2012-11-21
Last updated
2024-12-05

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01731444. Inclusion in this directory is not an endorsement.