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VistaCare® in the Treatment of Wounds of the Lower Extremity

NCT03790202 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2021-02-02

No results posted yet for this study

Summary

Assessment of the safety and performance of the VistaCare® medical device in current medical practice in the treatment of acute and chronic lower limb wounds.

Conditions

  • Wound Heal

Interventions

DEVICE

VistaCare®

Controlled atmosphere wound healing device

Sponsors & Collaborators

  • DTAMedical SAS

    lead INDUSTRY

Principal Investigators

  • Dominique Casanova, MD Pr · Hôpital de la Conception, Marseille, France

  • Regis Legré, MD Pr · Hôpital de la Timone, Marseille, France

  • Pierre-Edouard Magnan, MD Pr · Hôpital de la Timone, Marseille, France

  • Pascal Desgranges, MD Pr · CHU Henri Mondor, Créteil, France

  • Franck Duteille, MD Pr · CHU Nantes, France

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-02-18
Primary Completion
2020-12-31
Completion
2021-02-01

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 NCT03790202 on ClinicalTrials.gov