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

NCT02963519 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2016-11-15

No results posted yet for this study

Summary

Primary objective:

Demonstrate that in patients with acute leg wounds with skin defect, VistaCare® accelerates the formation of a quality granulation tissue and reduces preparation time to a cover gesture.

Secondary objectives:

* Evaluate the success of hedging gesture
* Assess the quality of the bud by colorimetry
* Assess tolerance
* Collect medical and economic data on the care of patients included
* Evaluate the quality of life of patients
* Assess patient comfort
* Evaluate the ease of use for the caregiver

Conditions

  • Leg Injury

Interventions

DEVICE

VistaCare®

DEVICE

Dressings

Sponsors & Collaborators

  • DTA Medical

    collaborator UNKNOWN

  • Qualissima

    lead OTHER

Principal Investigators

  • Dominique Casanova · APHM

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2016-11-30
Primary Completion
2017-11-30
Completion
2018-01-31

Countries

  • France

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 NCT02963519 on ClinicalTrials.gov