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Field Shield Wound Dressing Study

NCT07337616 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2026-01-13

No results posted yet for this study

Summary

This study is to compare the Field Shield Wound Dressing (FSWD) as a treatment for burn wounds to a standard of care burn wound dressing to evaluate healing, infection, pain/discomfort, and deepening of wound over time.

Conditions

  • Burn Wounds - Partial Thickness (2nd Degree)

Interventions

DEVICE

Field Shield Wound Dressing

Spray on wound dressing.

DEVICE

Silverlon

Silver dressing

Sponsors & Collaborators

  • Valleywise Health

    collaborator OTHER

  • United States Army Institute of Surgical Research

    collaborator FED

  • The University of Texas Health Science Center at San Antonio

    collaborator OTHER

  • KeriCure Medical

    lead INDUSTRY

Principal Investigators

  • Kerriann Greenhalgh, PH.D. · KeriCure Medical

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2025-05-01
Primary Completion
2026-07-30
Completion
2026-09-29
FDA Device
Yes

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 NCT07337616 on ClinicalTrials.gov