Reducing Wound Infections Using Bioelectric Wound Dressings

Part of paid clinical trials in Kissimmee, Florida.

Sponsor
AdventHealth
Study ID
NCT06312267
Status
Enrolling By Invitation

Conditions

  • Surgical Site Infection

Eligibility Criteria

Sex
ALL
Age
18 Years - 90 Years
Healthy Volunteers
Not accepted

Interventions

  • Bioelectric dressing — DEVICE
    Participants randomized into the experimental arm will have a bioelectric dressing applied 3 days before surgery, and 3 days post-surgery.

Study Details

The purpose of this study is to compare the outcomes of using Bioelectric wound dressing on the pre-operative wound site and post operatively and compared it outcomes to the standard of care chlorhexidine skin preparation.

Key Dates

Start date
Mar 4, 2024
Status verified
Apr 2026
Primary completion
May 1, 2026
Completion
May 1, 2026

Study Design

Enrollment
20 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • No Intervention: Control Arm
    Study participants will undergo surgery using current ERAS protocol standard of care skin cleaning preparation.
  • Experimental: Experimental Arm
    Study participants will use Bioelectrical dressing preoperatively and post-operative.

Primary Outcome Measure

Quantitative bacterial count [ Time Frame: 4 total biopsies will be collected. (3 days before surgery, surgery day pre incision, immediately post-surgery and 3 days post-surgery) ]

Locations (1)

FacilityCityStateZIPSite coordinators
AdventHealth CelebrationKissimmeeFlorida34747-

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AdventHealth Celebration· Kissimmee, FL

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