Modified Polyurethane Film Dressing For Skin Graft Donor Sites

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00600457

Enrollment

Registered

2008-01-25

Start date

2007-03-31

Completion date

2007-09-30

Last updated

2008-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wound Healing

Keywords

healing time, pain, infection

Brief summary

The purpose of this study is to determine whether the combination of modified polyurethane film and secondary absorbent dressing for skin graft donor sites avoids the regular uncontrolled leakage, but holds up the advantages of film dressings for this kind of wound.

Interventions

DEVICEPolyurethane Film

The modified polyurethane film is combined with a secondary absorbent dressing and remained intact until the 10th postoperative day

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Adults over age 18 who require skin grafting

Exclusion criteria

* Individuals under the age of 18.

Design outcomes

Primary

Measure	Time frame
uncontrolled leakage	1-10th day postoperative

Secondary

Measure	Time frame
pain	1-10th day postoperative
infection	1-10th day postoperative
epithelization status	10th day postoperative

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026