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Treatment of Cutaneous Ulcers With a Novel Biological Dressing

NCT00207818 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2014-02-11

No results posted yet for this study

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.

Conditions

  • Venous Ulcers

Interventions

DEVICE

self assembled skin substitute (SASS)

Wound care with self assembled skin substitute (SASS)

Sponsors & Collaborators

  • CHU de Quebec-Universite Laval

    lead OTHER

Principal Investigators

  • Francois A Auger, MD · Centre hospitalier affilié universitaire de Québec

  • Lucie Germain, Ph.D. · Centre hospitalier affilié universitaire de Québec

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1999-09-30
Primary Completion
2009-06-30
Completion
2009-06-30

Countries

  • Canada

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 NCT00207818 on ClinicalTrials.gov