RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

An Observational Clinical Registry to Collect Safety and Efficacy Data on Wound Care in Medical Centers

Quick Facts

Study Start:2019-02-14
Study Completion:2026-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04699305

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Subject is ≥18 years of age
  2. * Subject has an exuding cutaneous wound
  3. * Subject agrees to the use of his health data, including photos of his wound in analysis and publications
  4. * Subject/LAR must be able to read and understand English and/or Spanish
  1. * Subject/LAR is unable to read and understand English or Spanish.

Contacts and Locations

Study Contact

Sharon Sirota
CONTACT
+972545800765
sharon@reddress.co.il

Principal Investigator

Sharon Sirota
STUDY_DIRECTOR
RedDress Ltd.

Study Locations (Sites)

Wound Care Experts
Las Vegas, Nevada, 89128
United States

Collaborators and Investigators

Sponsor: RedDress Ltd.

  • Sharon Sirota, STUDY_DIRECTOR, RedDress Ltd.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-02-14
Study Completion Date2026-01-31

Study Record Updates

Study Start Date2019-02-14
Study Completion Date2026-01-31

Terms related to this study

Keywords Provided by Researchers

  • DFU, PU, Surgical, Vascular, Trauma

Additional Relevant MeSH Terms

  • Cutaneous Wounds