Post Marketing Trial for Evaluating the Effectiveness of ActiGraft in Treating Lower Extremity Hard To Heal Wounds

Not Applicable

Terminated

• Conditions: Wounds

• Registration Number: NCT04745806
• Lead Sponsor: RedDress Ltd.

Brief Summary

The study is a prospective, single arm, post- marketing study. The subjects enrolled to the study will receive weekly applications of ActiGraft until complete healing or until investigator's decision that patient can no longer benefit from the study treatment.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-02-04
• Study First Submitted QC: 2021-02-04
• Study First Posted: 2021-02-09
• Study Start: 2021-03-01
• Primary Completion: 2023-01-01
• Study Completion: 2023-01-01
• Status Verified: 2024-11
• Last Update Submitted: 2024-11-13
• Last Update Posted: 2024-11-15

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 6

Inclusion Criteria

1. Subject is ≥18 years of age
2. Patient with a chronic lower extremity ulcer (i.e DFU, VLU, ...)
3. Ulcer duration >30 days.
4. Ulcer size decreased in less than 30% in the 14 days prior to enrollment, while treated with standard of care (or advanced treatment)
5. Subject must be willing to comply with the protocol including having blood drawn to create the ActiGraft
6. Subject can read and understand the Informed Consent form

Exclusion Criteria

1. Presence of active underlying osteomyelitis.
2. Known malignancy in the reference wound bed or margins of the wound
3. Cannot withdraw blood in the required amount technically.
4. Subject is receiving (i.e., within the past 30 days) systemic steroids (more than 10mg per day)
5. Subject has been treated with wound dressings that include growth factors, engineered tissues or skin substitutes (within the past 30 days).
6. Subject has been treated with hyperbaric oxygen, wound VAC or Ozone gas(O3) within the past 5 days or is scheduled to receive during the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Percent of Reduction in Wound Size Over 12 Weeks	4, 8, and 12 weeks	The change in wound area (decrease or increase) with respect to the area at baseline, expressed as a percentage.

Secondary Outcome Measures

Name	Time	Method
Number of Participants Achieving a Complete re-epithelialization at 18 and 24 Weeks	18 and 24 weeks	Skin re-epithelialization without drainage or dressing requirements.
Number of Participants Achieving a Complete Wound Closure at 12 Weeks	12 weeks	Skin re-epithelialization without drainage or dressing requirements.
Percent of Reduction in Wound Size Over 18 and 24 Weeks.	18 and 24 weeks	The change in wound area (decrease or increase) with respect to the area at baseline, expressed as a percentage for wound treated beyond 12 weeks, per the investigator's decision
The change in wound pain by 12 weeks	12 weeks	Pain assessment would be done by using the Numeric Rating Scale (NRS). Subject chooses a number on a 1 to 10 scale that best describes his ulcer pain, while 0 represents "No Pain" and 10- " Worst Pain Imaginable "test, a scale between .

Trial Locations

Locations (1)

Emek Medical Center; 🇮🇱 Afula, Israel