Status:
COMPLETED
The Use of a Novel Microbicidal Liquid Polymer for the Reduction of Pin Track Infection
Lead Sponsor:
Prevent-Plus LLC
Conditions:
Infection
Post-operative Care
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
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 a...
Detailed Description
Study Objectives Research participants eligible for the study will be those undergoing Deformity Correction and Traumatic Provisional Fixation. These research participants have a number of pins placed...
Eligibility Criteria
Inclusion
- Deformity correction, traumatic provisional fixation
- All pin sites are stable
- 18 years of age or greater
- No known contraindication to receive product
Exclusion
- 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.)
Key Trial Info
Start Date :
November 7 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 30 2019
Estimated Enrollment :
13 Patients enrolled
Trial Details
Trial ID
NCT03756506
Start Date
November 7 2018
End Date
September 30 2019
Last Update
March 30 2021
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Julie Morris
St Louis, Missouri, United States, 63110