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Clinical and Histological Study of a Novel Dermal Substitute

NCT06255990 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 42

Last updated 2026-04-03

No results posted yet for this study

Summary

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.

Conditions

  • Skin Transplantation

Interventions

OTHER

Standard of care

Standard of care

Sponsors & Collaborators

  • University of Zurich

    collaborator OTHER

  • Kantonsspital Aarau

    collaborator OTHER

  • Kantonsspital Winterthur KSW

    collaborator OTHER

  • University Children's Hospital, Zurich

    lead OTHER

Principal Investigators

  • Sophie Böttcher, MD · University Children's Hospital, Zurich

Eligibility

Min Age
1 Year
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-15
Primary Completion
2026-06-01
Completion
2027-06-30

Countries

  • Switzerland

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 NCT06255990 on ClinicalTrials.gov