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ACTIVE NOT RECRUITING NA

Randomized Controlled Trial to Investigate Clinical Outcomes and Associated Costs When PermeaDerm is Used as Temporary Dressing for Surgical Wounds

NCT06750809 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this study is to compare the cost and clinical outcomes for two temporary dressings (Allograft and PermeaDerm) used in patients that need a skin graft to heal their wound. The researchers will review cost and other treatment results including how well both temporary dressings attach to the skin, how prepared the wound bed is to receive a skin graft, how long it takes for the skin to be ready to receive a skin graft, how well the skin graft takes and any complications. Patients will first have the temporary dressing applied to their wound, then a few days later, a skin graft will be performed. Patients will have photos of their wounds taken throughout the study including at all the clinic check-ups with the last check-up occurring about 8 weeks after treatment.

Interventions

  • DEVICE PermeaDerm Biosynthetic Wound Matrix
  • DEVICE Frozen Human Cadaveric Allograft (FHCA)

Study Locations (13)

Ohio

  • Akron Children's Hospital — Akron
  • Ohio State University — Columbus

Arizona

  • Valleywise Health — Phoenix

District of Columbia

  • Medstar Washington Hospital Center — Washington D.C.

Georgia

  • Grady Memorial — Atlanta

Iowa

  • Univ of Iowa — Iowa City

Kansas

  • University of Kansas — Kansas City

Kentucky

  • Univ of Louisville Burn Center — Louisville

Louisiana

  • University Medical Center — New Orleans

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2025-02-21
Est. Completion 2026-05
Phase NA

Sponsor

Avita Medical

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06750809

The ClinicalTrials.gov registry entry for NCT06750809 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Avita Medical, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Surgical Wound appearing as the primary indexed condition, and to 2 interventions — of which PermeaDerm Biosynthetic Wound Matrix is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06750809 reports 13 study locations spanning 12 distinct geographic areas — top geographies include Ohio, Arizona, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06750809 about?

NCT06750809 is a clinical study titled "Randomized Controlled Trial to Investigate Clinical Outcomes and Associated Costs When PermeaDerm is Used as Temporary Dressing for Surgical Wounds". The goal of this study is to compare the cost and clinical outcomes for two temporary dressings (Allograft and PermeaDerm) used in patients that need a skin graft to heal their wound. The researchers will review cost and other treatment results including how well both temporary dressings attach to t...

What is the current status of trial NCT06750809?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2025-02-21. Estimated completion is 2026-05.

What conditions does trial NCT06750809 study?

This clinical trial studies the following conditions: Surgical Wound, Trauma Wound, Partial-thickness Burn, Autografts, Partial Thickness Wounds. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06750809?

The interventions under investigation include: PermeaDerm Biosynthetic Wound Matrix (DEVICE), Frozen Human Cadaveric Allograft (FHCA) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06750809?

This trial is sponsored by Avita Medical, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06750809 being conducted?

This trial has 13 study locations across Arizona, District of Columbia, Georgia, Iowa, Kansas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial