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A Prospective Study Using SupraSDRM® in Promoting Healing and Reducing the Time to Grafting of Full-thickness Wounds

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 2 years 1 month later Oct 2025 → Dec 2027
See other at-risk trials from The Metis Foundation

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary completion pushed from Oct 2025 to Dec 2027v4 Show 4 more changesShow less
    • Recruitment opened
    • Start date changed from estimate of Mar 2025 to Jan 8, 2026
    • Study completion pushed from Oct 2026 to Dec 2027
    • Study sites: 0 to 1
  2. Primary completion date: Sep 2025 to Oct 2025
    • Study completion date: Sep 2025 to Oct 2026
    • Start date: Feb 2025 to Mar 2025
    • Collaborators: 1 to 3
    v3
  3. Start date: Sep 2024 to Feb 2025v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This is a prospective, randomized, controlled, multi-center clinical study comparing SupraSDRM® to standard of care wound dressing, BTM, in the treatment of full-thickness wounds deemed not immediately suitable for definitive grafting will be performed.
Trial Details
NCT Number NCT06503406
Lead Sponsor The Metis Foundation
Collaborators: The University of Texas Medical Branch, Galveston, United States Department of Defense, United States Army Institute of Surgical Research
Conditions
(from sponsor)		 Surgical Wound, Burns, Trauma Injury
Related terms Accidental Injuries, Burns, Surgical Wound
Enrollment 24 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov