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

Phase 1
Completed
Conditions
Burns
Wound Healing
Registration Number
NCT01061502
Lead Sponsor
Vomaris Innovations
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
17
Inclusion Criteria
  • Wounds resulting from skin graft
  • Split thickness wound
  • Wound size greater than 2x2 cm
  • Wounds must be ≥5 cm away from all other wounds
  • Participant agrees to participate in follow-up evaluation
  • Participant must be able to read and understand informed consent, and sign the informed consent
Exclusion Criteria
  • Concurrent participation in another clinical trial that involves an investigational drug or device that would interfere with this study
  • Participant is to receive another topical antimicrobial agent other than the study dressing
  • Participant with sensitivity or adverse reactions to silver or zinc
  • Pregnancy or nursing an infant or child
  • Immunosuppression
  • Active or systemic infection
  • Peripheral vascular occlusive disease
  • Collagen vascular disease
  • Connective tissue disease
  • Participant undergoing active cancer chemotherapy
  • Chronic steroid use
  • Decision impairment

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
To compare epithelialization over time3 months
Secondary Outcome Measures
NameTimeMethod
To compare patient reported perception of pain3 months
To compare scarring3 months

Trial Locations

Locations (1)

Blodgett Hospital

🇺🇸

Grand Rapids, Michigan, United States

Blodgett Hospital
🇺🇸Grand Rapids, Michigan, United States

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