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

NCT01430130 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2014-11-28

Study results available
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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

  • Neodyne Biosciences, Inc.

    lead INDUSTRY

Principal Investigators

  • Jennifer Weintraub, MD · Duet Plastic Surgery

  • Angeline Lim, MD · Duet Plastic Surgery

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2011-09-30
Primary Completion
2012-11-30
Completion
2012-11-30

Countries

  • United States

Study Locations

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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 NCT01430130 on ClinicalTrials.gov