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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

Overview

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.