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Clinical and Histological Study of a Novel Dermal Substitute

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated April 3, 2026 (before its estimated June 1, 2026 completion). Its status may not reflect the trial's current state.

Record History

See every version on ClinicalTrials.gov ↗

  1. Eligibility criteria shortened, about 16 words
    • Site contacts updated at 1 of 4 sites
    v6
  2. Eligibility criteria revisedv5
  3. Study sites: 2 to 4
    • Collaborators: 1 to 3
    v4
  4. Primary completion date: Jun 2026 to Jun 1, 2026
    • Site contacts updated at 2 of 2 sites
    v3
  5. Site contacts updated at 2 of 2 sitesv2
  6. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
The goal of this observational study is to compare a novel dermal substitute to a the current standard procedure in the treatment of full thickness skin defects. The main questions aim to answer are: • Is the skin elasticity treated with the novel dermal substitute better than the skin elasticity treated with the current standard procedure Participants skin elasticity will be measured by Cutometer® MPA-580 assessment.
Trial Details
NCT Number NCT06255990
Lead Sponsor University Children's Hospital, Zurich
Collaborators: University of Zurich, Kantonsspital Aarau, Kantonsspital Winterthur KSW
Conditions
(from sponsor)		 Skin Transplantation
Enrollment 42 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov