Clinical Trials Directory

Trials / Completed

CompletedNCT01430130

Investigation of a Novel Silicone Dressing to Maximize the Outcomes of Scar Revision Procedures (IMPROVE)

Investigation of a Novel Mechanomodulating Polymer to Maximize the Outcomes of Scar Revision Procedures

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Neodyne Biosciences, Inc. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Neodyne has developed an investigational dressing for post-operative incision care. Neodyne is conducting this research to study whether the investigational dressing, called the Neodyne Dressing, can minimize scar formation in a simple manner.

Detailed description

It is proposed to study a dressing designed to reduce the appearance of scars after scar revision surgery. It is expected that by managing the incision site after primary closure but during the longer term healing phase, scar formation may be minimized.

Conditions

Interventions

TypeNameDescription
DEVICEembrace deviceAdhesive bandage/dressing intended to minimize scar formation.

Timeline

Start date
2011-09-01
Primary completion
2012-11-01
Completion
2012-11-01
First posted
2011-09-07
Last updated
2014-11-28
Results posted
2014-11-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01430130. Inclusion in this directory is not an endorsement.

Investigation of a Novel Silicone Dressing to Maximize the Outcomes of Scar Revision Procedures (IMPROVE) (NCT01430130) · Clinical Trials Directory