Evaluation of Improved Preparation Time to a Coverage in Patients With Acute Wounds by Use of VistaCare® Versus Dressings

Recruitment & Eligibility

Inclusion Criteria

Man or woman
Age from 18 to 65 inclusive
Patient with acute or leg sores (s), traumatic, with skin defect with or without external fixators and without exposure to fine fabrics (functional tendon, artery, vessel, bone, osteosynthesis material ...). These wounds may be burns, deep second degree only.
Patient having no associated pathology
Patient has given its written consent, lighting, dated and signed
Patient affiliated to a social security scheme
Voluntary Patient and able to comply with the protocol requirements
Patient whose wound is located below the knee
Patient whose wound date of less than 2 weeks
A patient whose wound has a minimum area of 10 cm2
Patient whose wound does not require surgical debridement after inclusion (if surgical debridement is necessary, it must be performed before inclusion in the study)

Exclusion Criteria

Pregnant or breastfeeding women
Women of childbearing potential not using effective contraception (combined hormonal, IUD) and failing achieving a pregnancy test and getting the result before starting treatment
Patients do not speak and do not read French
Patient with one or more risk factors such as smoking more than 5 cigarettes a day, diabetes, autoimmune disease
Patients with such treatment during or within one month prior to inclusion in the study: corticosteroids, topical corticosteroids at the immunosuppressive wound or radiotherapy
A patient whose wound is located at a place not compatible with the use of VistaCare®
Patient with traumatic wound leg with exposure to some tissues (functional tendon, artery, vessel, bone, osteosynthesis material ...)
Patient with general signs of infection (temperature, lymphangitis, osteitis proven)
Patient with a bleeding wound
Patient with a burn to a stage other than deep second degree
Patients with a wound whose area is less than 10 cm2
Patient with a plague of nontraumatic leg
Previous participation in this trial
Patient in exclusion period from another clinical trial or participated in a clinical trial in the month before inclusion
Patient whose wound is more than 2 weeks
Patient whose wound was treated by hyperbaric chamber

Study & Design

Arm && Interventions

Group	Intervention	Description
VistaCare®	VistaCare®	VistaCare® Medical device for treatment into an editable atmosphere
Dressings	Dressings	Dressings Adapted to the case

Primary Outcome Measures

Name	Time	Method
Quality of the bud	Change from inclusion day at Day 15 of the quality of the bud	Comparison, after the inclusion in the study, between VistaCare® and dressings on preparation time to a cover gesture by daily visual assessment of the quality of the bud.

Secondary Outcome Measures

Name	Time	Method

Recruitment & Eligibility