Using phenylephrine to reduce blood loss during burn surgery
Official title: Phenylephrine Tumescence for Hemostasis in Surgery for Burn Injury - A Randomized Control Trial
Run by University of Manitoba · NCT01731444 · Data updated 2026-11-12
This study is testing if phenylephrine can help reduce blood loss during burn surgery without affecting heart rate or blood pressure.
Quick facts
| Phase | Phase 1 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 24 (estimated) |
| Sponsor | University of Manitoba Academic / other |
| Locations | 1 site (Winnipeg, Manitoba) |
| Status | Recruiting |
| Started | December 1, 2014 |
| Main results expected | June 1, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | May 14, 2026 |
| Trial ID | NCT01731444 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals with burn injuries requiring debridement and grafting covering 5-30% of total body surface area.
✕Probably not a fit
Patients with burns on the head, neck, hands, feet, or genitals, or those with certain cardiovascular conditions or on specific medications may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates the use of phenylephrine as an alternative to epinephrine for controlling blood loss during skin grafting in burn injuries. The study aims to determine if phenylephrine can effectively reduce blood loss without causing adverse effects on heart rate or blood pressure. Participants will receive injections of phenylephrine under the skin at the site of injury before undergoing standard surgical procedures. The goal is to evaluate the safety and efficacy of phenylephrine in this context.
Why it matters
Potential benefit: If successful, this approach could lead to safer surgical procedures for burn victims by minimizing blood loss without impacting cardiovascular function.
How similar studies have gone: While the use of epinephrine is standard in similar procedures, the application of phenylephrine in this context is novel and has not been extensively tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria a) Burn injury requiring debridement and grafting between 5-30% TBSA Exclusion Criteria 1. Head and neck, hand, foot, or genital burns 2. On anticoagulants (except NSAIDs) 3. On monoamine oxidase inhibitor or tricyclic antidepressant 4. Coronary or peripheral vascular disease 5. History of arrhythmias 6. On a Beta-blocker 7. History of vascular abnormality 8. Hypertension
Where it's running
-
University of Manitoba
Winnipeg, Manitoba, Canada Recruiting
Study contacts
- Study coordinator: Justin Gawaziuk, MSc
- Email: jgawaziuk@hsc.mb.ca
- Phone: 2047873669
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.