Safety and Efficacy of ActiGraft Treatment in Wound Care in Medical Centers
NCT04699305 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500
Last updated 2025-07-29
Summary
Multicenter observational study to explore the efficacy of ActiGraft in the treatment of exuding cutaneous wounds in real-life usage.
Conditions
- Cutaneous Wounds
Interventions
- DEVICE
-
ActiGraft
Whole blood clot (WBC) gel
Sponsors & Collaborators
-
RedDress Ltd.
lead INDUSTRY
Principal Investigators
-
Sharon Sirota · RedDress Ltd.
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-02-14
- Primary Completion
- 2026-07-01
- Completion
- 2027-01-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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