Evaluation of the Safety Performance of 3M Tegaderm Finishing Dressing

The objective of this study is to eavluate the safety performance of Tegarderm™ Finishing Dressing when worn on various chronic wounds for up to four weeks of treatment.

Inclusion Criteria

• Subjects with wounds that have low to moderate wound exudate
• Subjects who have a full thickness granulated wound or partial thickness wound with dermis exposed
• Wound area of at least 2.0 cm²

Exclusion Criteria

• Subjects who have peripheral neuropathy at the wound location
• Subjects who have used a cellular tissue based product in the past 4 weeks
• Subjects with a full thickness burn

Study Requirements

Subjects will be followed for up to four weeks with two visits per week.