Overview

The Effect of Topical Tranexamic Acid on Postoperative Bleeding From Superficial Wounds

Status:
Recruiting
Trial end date:
2022-03-01
Target enrollment:
0
Participant gender:
All
Summary
After surgical procedures, interventions to reduce postoperative bleeding are of great importance. In this study, the effect will be investigated of administering tranexamic acid, which is designed for injection, directly onto the raw wound surface (topical application) created during surgery. In this way only a small amount of drug is to reach a large wound area. There will be a higher drug concentration of it in the exposed wound surface than after injection, but only a very low concentration in the body, and no risk of injury from needles. The researchers have recently shown that topically applicated tranexamic acid reduces bleeding in women who had two-sided breast reduction surgery. Now it will be studied whether topically applicated tranexamic acid reduces bleeding from superficial wounds, using as a study model the homogenous wounds created by tangential skin excision when harvesting split skin grafts for skin transplants. Two identical wound surfaces in the same patient will serve as case and control.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
St. Olavs Hospital
Collaborator:
Haukeland University Hospital
Treatments:
Tranexamic Acid
Criteria
Inclusion Criteria:

- to undergo split skin graft harvesting

- two equally large and symmetrically distributed wounds can be defined in the donor
area

- received adequate oral and written information about the study and signed an
informed-consent form. For those not capable of giving informed consent at the time of
inclusion but included via next-of-kin, consent will be obtained or withdrawn when the
patient is able to independently consider the inclusion

Exclusion Criteria:

- pregnant or breastfeeding

- known allergy to tranexamic acid/Cyklokapron®