Study to Evaluate the Effect of Sorbion Sachet S Wound Dressing

Status Completed

Clinical Trial Summary

This is a clinical study to evaluate the effects of sorbion sachet s wound dressing on soft tissue edema and wound bioburden in moderately to highly exuding pressure ulcers.

Clinical Trial Description

This study is aimed at the participation of subject with moderately to highly exuding pressure ulcers. Each Subject is expected to participate for a period of 4 weeks or until reepithelization, which occurs first. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01319097
Study type	Interventional
Source	Southwest Regional Wound Care Center
Contact
Status	Completed
Phase	N/A
Start date	April 2010
Completion date	August 2011

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