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Clinical Trial Summary

The primary objective of this study is to evaluate the safety and preliminary performance of EASH dressing for 4 weeks followed by AQUACEL® dressing for 4 weeks on venous leg ulcers.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01497210
Study type Interventional
Source ConvaTec Inc.
Contact
Status Completed
Phase Phase 2
Start date November 2011
Completion date April 2012

See also
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