Avita Medical Ltd ((RCEL)) announced an update on their ongoing clinical study.
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Avita Medical Ltd is conducting a clinical study titled ‘A Prospective Post-Market Multicenter Randomized Controlled Clinical Study to Investigate Clinical Outcomes and Associated Costs When PermeaDerm is Used as Temporary Dressing for the Management of Surgical Wounds’. The study aims to evaluate the clinical outcomes and economic impact of using PermeaDerm compared to Frozen Human Cadaveric Allograft (FHCA) as temporary dressings for surgical wounds requiring skin grafts. This research is significant as it could influence treatment protocols and cost-effectiveness in wound care management.
The interventions being tested are PermeaDerm Biosynthetic Wound Matrix and Frozen Human Cadaveric Allograft (FHCA), both used as temporary dressings before skin graft procedures. These devices are intended to prepare the wound bed and support the grafting process.
This is a randomized, parallel-assignment study with no masking, primarily focused on treatment outcomes. Patients are randomly assigned to receive either PermeaDerm or FHCA, and the study aims to compare their effectiveness and cost implications.
The study began on February 21, 2025, with primary completion expected shortly after. The last update was on July 8, 2025. These dates are crucial for tracking the study’s progress and anticipating results.
Market implications of this study could be significant for Avita Medical’s stock performance, as positive results may enhance investor confidence and position the company favorably against competitors in the wound care industry. The study’s findings could also influence market dynamics by setting new standards in surgical wound management.
The study is currently ongoing, with further details available on the ClinicalTrials portal.