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Trials / Completed

CompletedNCT01055925

Clinical Comparative Trial of a Modified Polyurethane Dressing and Aquacel

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
Sponsor
Klinik Bogenhausen · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers

Summary

The almost single disadvantage of conventional polyurethane film dressings, an uncontrolled leakage, is probably as often described as its numerous advantages for split-thickness skin graft (STSG) donor sites. This shortcoming can be overcome by perforating the polyurethane dressing (MPD), which permits a controlled leakage into a secondary absorbent dressing. The study was conducted to compare the MPD-system and Aquacel® (ConvaTec), a hydrofiber wound dressing, which also seems to fulfill all criteria of an ideal donor site dressing.

Conditions

Interventions

TypeNameDescription
DEVICEmodified polyurethane film dressing (OpSite, Smith&Nephew, London, UK)
DEVICEAquacel® (ConvaTec, Skillman, NJ, USA), sodium carboxy-methylcellulose hydrocolloid polymer dressing

Timeline

First posted
2010-01-26
Last updated
2010-01-26

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01055925. Inclusion in this directory is not an endorsement.

Clinical Comparative Trial of a Modified Polyurethane Dressing and Aquacel (NCT01055925) · Clinical Trials Directory