Safety and Efficacy of ActiGraft Treatment in Wound Care in Medical Centers

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRedDress Ltd.

About this trial

Multicenter observational study to explore the efficacy of ActiGraft in the treatment of exuding cutaneous wounds in real-life usage.

Eligibility criteria

Qualifiers

Subject is ≥18 years of age

Subject has an exuding cutaneous wound

Subject agrees to the use of his health data, including photos of his wound in analysis and publications

Subject/LAR must be able to read and understand English and/or Spanish

Disqualifiers

Subject/LAR is unable to read and understand English or Spanish.

Trial design

Treatments tested in this trial

  • ActiGraft

Treatment groups

500 Participants
are divided into 1 treatment group

Sponsors and collaborators