Treatment of Cutaneous Ulcers With a Novel Biological Dressing

Status Completed

Clinical Trial Summary

The aim of the study is to evaluate the effect of a biological dressing on the healing process of venous ulcers. The dressing is a reconstructed skin substitute made with the patients own cells.

Clinical Trial Description

The hypothesis of this trial is that the cutaneous model SASS, a dermal epidermal skin substitute, created by the LOEX could be as high-performant, or even better, than the one's already existent in North America for the wound care. We anticipate showing on 6 patients that ulcer that did not close with conventional treatment, will heal or at least improve with this treatment. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00207818
Study type	Interventional
Source	Centre Hospitalier Universitaire de Québec, CHU de Québec
Contact
Status	Completed
Phase	Phase 1/Phase 2
Start date	September 1999
Completion date	June 2009

View Details

See also
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