Share on facebook Share on Twitter Share on Google Plus Share This
Back to Results

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.

Study Details

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.