VeraFlo With Prontosan® and Wound and Fracture Healing.
Stopped early · Not applicable
Conditions studied: Infection
In brief
To answer the question: "Do Prontosan instillations decrease time to wound and fracture healing and decrease bacterial load compared to wound vac treatment without Prontosan?," we will enroll up to 30 subjects (for an anticipated 20 complete data sets) into this trial. The subjects will be split equally into two different groups by randomization. One groups will have wound vac therapy with Prontosan, and one group will have wound vac therapy without Prontosan. Data related to wound and fracture healing and bacterial load will be assessed between the two groups to determine if wound vac therapy with Prontosan speeds up healing time and decreases bacterial load.
Key facts
- Study ID
- NCT02621073
- Run by
- Brett Crist
- People needed
- 7
- Starts
- 2015-11-01
- Expected to finish
- 2017-12-01
- Last updated by the study team
- 2019-06-20
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients 18 years and older
- Patients who will be undergoing surgical management (including the use of NPWT therapy) of an infected lower extremity status-post open reduction and internal fixation (ORIF)
You may not qualify if…
- Pregnant females
- Incarcerated patients and those not able to give informed consent
Where it is running
- University of Missouri — Columbia, Missouri, United States
Full record on ClinicalTrials.gov
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