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Evaluation of the Safety Performance of 3M Tegaderm Finishing Dressing
Title |
Evaluation of the Safety Performance of 3M Tegaderm Finishing Dressing |
Therapeutic Area |
Wound Care
|
Principal Investigator |
Mark Iafrati, MD |
Min Age |
18 Years |
Gender |
All |
Contact |
Kaytie Beasley 617 636-5287 |
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.