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CompletedNCT01591434

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

An Open Randomised Comparative Study to Evaluate the Performance of AQUACEL® Extra™ in Venous Leg Ulcers

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
65 (actual)
Sponsor
ConvaTec Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEAQUACEL®Dressing to be changed as clinically needed or at least every seven days.
DEVICEAQUACEL® Extra™Dressing to be changed as clinically needed or at least every seven days.

Timeline

Start date
2012-05-01
Primary completion
2012-09-01
Completion
2012-09-01
First posted
2012-05-04
Last updated
2013-07-30

Locations

12 sites across 4 countries: Germany, Netherlands, Poland, United Kingdom

Source: ClinicalTrials.gov record NCT01591434. Inclusion in this directory is not an endorsement.

Study to Evaluate the Performance of AQUACEL® Extra™ in Venous Leg Ulcers (NCT01591434) · Clinical Trials Directory