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

PHASE3CompletedINTERVENTIONAL
Enrollment

65

Participants

Timeline

Start Date

May 31, 2012

Primary Completion Date

September 30, 2012

Study Completion Date

September 30, 2012

Conditions
Leg Ulcer
Interventions
DEVICE

AQUACEL®

Dressing to be changed as clinically needed or at least every seven days.

DEVICE

AQUACEL® Extra™

Dressing to be changed as clinically needed or at least every seven days.

Trial Locations (12)

79100

Dermatologische Gemeinschaftspraxis, Freiburg im Breisgau

Unknown

Bramfelder Chaussee, Hamburg

6401 CX

Mitralis Expertise Centrum, Heerlen

90-553

Nzoz Certus, Lodz

03-983

CF Centrum Flebologii Anna i Beata Narojczyk, Warsaw

18, 02-366

Continuum Care, Warsaw

41-819

"Medyczna Medservice", Zabrze

CH49 5PE

Arrowe Park Hospital,, Upton

BD9 6RJ

Bradford Teaching Hospitals, Bradford

CF14 4XN

Wound Healing Research Unit, Cardiff University, Cardiff

BN21 4RL

Tissue Viability Consultancy Services Ltd, Eastbourne

WV12 5PR

Walsall Healthcare NHS Trust Short Heath Clinic, Willenhall

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ConvaTec Inc.

INDUSTRY

NCT01591434 - Study to Evaluate the Performance of AQUACEL® Extra™ in Venous Leg Ulcers | Biotech Hunter | Biotech Hunter