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The Effect of Wound Irrigation With Irrisept on Abscess Healing (Irrisept UF Study)

Abscess Clinical Trial

Official title:
The Effect of Wound Irrigation With Irrisept Delivery System on Abscess Healing in Patients Presenting to the Emergency Department

Clinical Trial Summary

The purpose of this study was to evaluate the safety and effectiveness of Irrisept compared to standard of care treatment of skin and soft tissue infections in the form of abscesses.

Clinical Trial Description

After being informed about the trial and potential risks, subjects completed an informed consent form prior to participation. After eligibility criteria was verified, an initial wound assessment examination was performed. Subjects were then randomized to the Irrisept or Standard of Care treatment group. At intervals of 48 hours (up to 96 hours) later, abscesses were assessed until healing occurred. If the subject required antibiotics, this was recorded, as well as results from the wound and Methicillin-resistant Staphylococcus Aureus (MRSA) cultures. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04957732
Study type Interventional
Source Irrimax Corporation
Contact
Status Terminated
Phase N/A
Start date January 2010
Completion date November 2011
View Details
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