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Efficacy Study of a Bioelectric Dressing to Treat Skin Graft Donor Site Wounds

NCT01061502 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 17

Last updated 2010-12-10

No results posted yet for this study

Summary

The purpose of this study is to determine whether the use of a bioelectric wound dressing is effective in the healing of skin graft donor site wounds.

Conditions

  • Burns
  • Wound Healing

Interventions

DEVICE

Procellera (Bioelectric Wound Dressing)

Dressing used on one-half of the donor graft site. Dressing changes every 5-7 days, more frequently if needed

DEVICE

Opsite (Transparent Adhesive Dressing)

Semi-occlusive wound dressing placed on one-half of the skin graft donor site. Dressing change every 5-7 days, more frequently if needed.

Sponsors & Collaborators

  • Vomaris Innovations

    lead INDUSTRY

Principal Investigators

  • Andrew L Blount, MD · Blodgett Hospital

  • Richard Wilcox, MD · Blodgett Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2010-11-30
Completion
2010-11-30

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 NCT01061502 on ClinicalTrials.gov