Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Pressure Ulcer
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Single (Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

The secondary objectives of this study are to compare the following items between the two arms of the study: A. The evolution of skin microbiota in the wound B. The evolution of the surface and the depth of the wound during follow-up C. The healing process D. Patient and caretaker acceptability

The secondary objectives of this study are to compare the following items between the two arms of the study: A. The evolution of skin microbiota in the wound B. The evolution of the surface and the depth of the wound during follow-up C. The healing process D. Patient and caretaker acceptability

Tracking Information

NCT #
NCT02373956
Collaborators
MELIPHARM SAS
Investigators
Principal Investigator: Jean-Philippe Lavigne, MD, PhD Centre Hospitalier Universitaire de Nîmes