MedTrace Logo

A Study of a Novel Silicone Dressing to Minimize Scar Formation

NCT01399099 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 67

Last updated 2024-11-19

Study results available
· View outcomes & findings →

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.

Conditions

  • Hypertrophic

Interventions

DEVICE

embrace device

Adhesive bandage/dressing intended to minimize scar formation.

Sponsors & Collaborators

  • U.S. Army Medical Research and Development Command

    collaborator FED

  • Neodyne Biosciences, Inc.

    lead INDUSTRY

Principal Investigators

  • Rodney J Rohrich, MD, FACS · University of Texas Southwestern Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2012-09-30
Completion
2013-03-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01399099 on ClinicalTrials.gov