Evaluating ActiGraft for treating cutaneous wounds
An Observational Clinical Registry to Collect Safety and Efficacy Data on Wound Care in Medical Centers
This study is testing if ActiGraft can help heal different types of wounds, like diabetic foot ulcers and pressure sores, in real-life situations.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | RedDress Ltd. Industry-sponsored |
| Locations | 1 site (Las Vegas, Nevada) |
| Trial ID | NCT04699305 on ClinicalTrials.gov |
What this trial studies
This multicenter observational study aims to assess the safety and efficacy of ActiGraft in treating exuding cutaneous wounds in real-world settings. Participants will be monitored for their wound healing progress while receiving ActiGraft treatment. The study will collect health data and photographs of the wounds to analyze the outcomes effectively. The focus is on various types of wounds, including diabetic foot ulcers, pressure ulcers, surgical wounds, and trauma-related injuries.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older with exuding cutaneous wounds who can provide consent for data usage.
Not a fit: Patients who cannot read or understand English or Spanish may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly improve healing outcomes for patients with chronic and exuding wounds.
How similar studies have performed: While this approach is being evaluated in a real-world context, similar studies have shown promise in wound care treatments.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * Subject/LAR is unable to read and understand English or Spanish.
Where this trial is running
Las Vegas, Nevada
- Wound Care Experts — Las Vegas, Nevada, United States (Recruiting)
Study contacts
- Study coordinator: Sharon Sirota
- Email: sharon@reddress.co.il
- Phone: +972545800765
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.