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

Part of paid clinical trials in Las Vegas, Nevada.

Sponsor: RedDress Ltd.
Study ID: NCT04699305
Status: Recruiting

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Conditions

Cutaneous Wounds

Eligibility Criteria

Sex: ALL
Age: 18 Years - N/A
Healthy Volunteers: Not accepted

Interventions

ActiGraft — DEVICE
Whole blood clot (WBC) gel

Study Details

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

Key Dates

Start date: Feb 14, 2019
Status verified: Jul 2025
Primary completion: Jul 1, 2026
Completion: Jan 31, 2027

Study Design

Enrollment: 500 participants (estimated)

Arms

Arm: ActiGraft
Whole blood clot (WBC) gel

Primary Outcome Measure

Percentage area reduction (PAR) at 4 weeks [ Time Frame: 4 weeks ]

Central Contacts

Sharon Sirota
+972545800765
[email protected]

Locations (1)

Facility	City	State	ZIP	Site coordinators
Wound Care Experts	Las Vegas	Nevada	89128	Naz Wahab, M.D

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Wound Care Experts· Las Vegas, NV