A Dual-center Study Evaluating Clinical Acceptance of a NPWT Wound Care

Status Completed

Clinical Trial Summary

The purpose of this study is to determine if use of the Medela Invia Motion NPWT system supports acceptable progress towards the goal of therapy when treating patients with a variety of wound types during the evaluation period.

Clinical Trial Description

The primary objective is to evaluate whether clinical opinion of product performance results in expected wound response and outcomes when using the Medela Invia Motion Endure NPWT system during 4-week study duration. * Goal of therapy will be defined by the physician according to initial assessment: Endpoints (dependent on goal of therapy): - Decrease in wound volume - Decrease in size of the tunneling area - Decrease in size of undermining - Decrease in amount of slough - Increase in granulation tissue - Decrease in edema/periwound swelling - The wound bed is progressing acceptably towards a transition to another treatment modality such as Moist Wound Healing (MWH), surgical closure, or a flap or graft. **Study endpoint will be determined by physician at the time of enrollment, when the goal of therapy is documented** ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04593693
Study type	Interventional
Source	Medela AG
Contact
Status	Completed
Phase	N/A
Start date	December 10, 2020
Completion date	May 18, 2021

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A Dual-center Study Evaluating Clinical Acceptance of a NPWT Wound Care System

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms