Study to Evaluate the Performance of AQUACEL® Extra™ in Venous Leg Ulcers

Status Completed

Clinical Trial Summary

Based upon the in-vitro data AQUACEL® Extra™ achieves a 39% increase in absorbency. As such it is anticipated that through improved exudate management a longer wear time will be achieved in the AQUACEL® Extra™ group compared to AQUACEL® in the management of chronic wounds such as venous leg ulcers.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01591434
Study type	Interventional
Source	ConvaTec Inc.
Contact
Status	Completed
Phase	Phase 3
Start date	May 2012
Completion date	September 2012

View Details

See also
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