The Use of a Novel Microbicidal Liquid Polymer for the Reduction of Pin Track Infection

Completed · Not applicable

Conditions studied: Infection, Post-operative Care

In brief

The purpose of the study is to investigate additional clinical uses for the polymer, which 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 13 subjects will take part in this study.

Key facts

Study ID

NCT03756506

Run by

Prevent-Plus LLC

People needed

13

Starts

2018-11-07

Expected to finish

2019-09-30

Last updated by the study team

2021-03-30

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Deformity correction, traumatic provisional fixation
• All pin sites are stable
• 18 years of age or greater
• No known contraindication to receive product

You may not qualify if…

• Age less than 18 years
• Known allergy to Methylene Chloride
• Known sensitivity to organic polymers
• Non-clean, dry wound at pin
• Vulnerable research participants (Institutionalized, students, employees, prisoners, or those with decisional incapacity, etc.)

Where it is running

• Julie Morris — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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