DuraDerm® for the Reduction of Pin Track Infection
common.study.values.description
“DuraDerm® for the Reduction of Pin Track Infection”
The purpose of the study is to investigate additional clinical uses for DuraDermAR. DuraDermAR is a FDA approved, 510k, medical device, but has not been approved for use on patients with pin track sites as a way to lower the infection rate and is investigational for this purpose. The approved uses include wound care and post-operative care. About 20 subjects will take part in this study.
common.study.values.location
participant.ui.study.affiliations-map.online-study.header-virtual
participant.ui.study.affiliations-map.online-study.text
common.study.values.methods
common.study.methods.has-drugs-no
common.study.methods.is-healthy-no
Device - DuraDerm
DuraDerm® is a 510K FDA cleared medical device indicated for providing a covering over minor wounds and scrapes that are clean and dry. The microbicidal liquid solution consists of organic polymers . The unique formulation eradicates any organisms (bacteria, fungi, viruses) it comes in contact with. This is a result of the solvent's activity against an infinite number of organisms After eradication is complete, the solvent then transitions into a clear, elastomeric, non-odorous film for coverin ...read more on ClinicalTrials.org
participant.views.study.view.additional
participant.views.study.view.scientific-title
An Evaluation of the Use of DuraDerm® for the Reduction of Pin Track Infection in Research Participants Receiving External Fixation Following Deformity Correction and Traumatic Provisional Fixation
common.study.values.clinical-trial-id
NCT03756506
participant.views.study.view.id
bo2Aza
