Efficacy of ProgenaMatrix™ in the Management of DFUs

A Controlled Data Collection and Prospective Treatment Study to Evaluate the Efficacy of ProgenaMatrix™ in the Management of Diabetic Foot Ulcers

This multicenter study will collect data to determine closure time for diabetic ulcers when following protocol parameters and treatment with ProgenaMatrix™.

Study Overview

• Status: Active, not recruiting
• Conditions: Diabetic Foot Ulcer
• Intervention / Treatment: Device: ProgenaMatrix Keratin graft; Other: standard of care

Detailed Description

This is a multicenter data collection and treatment study with weekly updates to include pre and post debridement measurements of wound area, photographs and additional comments of wound appearance, exudate, and patient compliance. ProgenaMatrix™ will be used as the dressing to maintain a moist wound environment post-debridement. ProgenaMatrix™ is US Food and Drug Administration (FDA) cleared for the treatment of diabetic foot ulcers. The standard of care for diabetic foot ulcers (DFU) is removal of non-viable tissue, control of infection, maintain a moist wound environment and off-load the ulcer site. All aspects of this research are within the standard of care practice for the treatment of diabetic foot ulcers.

The use of ProgenaMatrix™ instead of a traditional dressing to maintain a moist healing wound environment is the only research intervention. Data on any adverse events related to treatment with ProgenaMatrix™ will be collected for research purposes.

The data in this study will be collected from subjects with controlled eligibility. The rationale for this control is to provide a real-world data set on subjects that have had their controllable comorbidities attenuated. This is good clinical practice at advanced wound treatment centers. This data will be statistically evaluated to provide a true closure rate when using ProgenaMatrix™ in a subject where standard of care treatments and assessments are followed. As with any good data set the control of as many variables as possible should provide a more consistent closure rate. This type data is not achievable in an observational study.

As the investigators move into randomized controlled trials, the investigators will maintain these criteria as the investigators strive to develop a predictive healing model when all aspects of patient care are considered. This will include which advanced dressing would be best applied to the wound based on patient status using an Artificial Intelligence program under development.

The investigators will also be looking at historical data on wound closure rates for traditional dressing as well as other advanced dressings that has been collected with similar eligibility criteria. All data input into our model will be controlled by similar eligibility requirements. This data will also be used as historical control for this study.

• Study Type: Interventional
• Enrollment (Actual): 100
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Washington
    • Puyallup, Washington, United States, 98371
      • United Wound Healing

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Understands and agrees that the standard treatment protocol will include the application of ProgenaMatrix™ as the standard of care for this project.
• Have participated in the informed consent process and signed a data collection and treatment specific informed consent.
• Be able and willing to comply with the data collection procedures, data collection visits, dressings, and off-loading.
• Have type I or type II diabetes mellitus with an Investigator-confirmed glycosylated hemoglobin (HBA1c) of less than or equal to 11.5% within 3 months prior treatment.

• Have at least one DFU Ulcer that has been in existence for a minimum of 4 weeks but no more than 12 months and meets all the following criteria:

  • Ulcer is partial or full thickness without capsule/tendon/bone exposure.
  • Ulcer is on the foot or ankle.
  • Ulcer area is greater than 1 sq. cm. but less than 18 sq. cm. post debridement. (Ulcers larger than 18 sq. cm. can be included with the approval of the Medical Monitor.)
  • If the subject has more than one ulcer the data collection ulcer will be at the discretion of the Investigator.
  • There is minimum of 1 cm between the ulcer treated and any other ulcer on the same foot.

• Have adequate vascular perfusion of the affected limb as defined by one of the following in order of preference.

  • Ankle-Brachial index of greater than .65 and less the 1.3
  • Toe Pressure of greater than 40 mmHg
  • TcPO2 of greater than 40 mmHg
• Patient had vascular re-perfusion more than 30 days prior to inclusion in the study.

Exclusion Criteria:

• The study ulcer has unexplored tunneling, undermining, or sinus tracts.
• The patient is unable to safely ambulate with appropriate off-loading device.
• The patient has a known sensitivity to the suggested dressings.
• The patient has or is suspected of having gangrene, wound infection, necrosis, redness, pain, purulent drainage or is being treated by antibiotic for the treatment of the above.
• The patient has confirmed osteomyelitis of the foot with the ulcer.
• The patient is on steroid therapy, immunosuppressive or autoimmune therapy, radiation therapy of the foot, thrombosis.
• History of bone of metastatic disease of the affected limb, radiation therapy or chemotherapy within 12 months prior to treatment.
• Pregnancy
• The patient is affected by any disease other than diabetes that can impair wound healing in the opinion of the Investigator.
• The patient has unstable Charcot with bony prominence that will inhibit wound healing.
• Excessive lymphedema that will inhibit off-loading.
• Is unwilling to allow the use ProgenaMatrix™ as the standard of care for this data collection project.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Treatment with ProgenaMatrix; application of ProgenaMatrix daily for 12 weeks	Device: ProgenaMatrix Keratin graft; place ProgenaMatrix graft on the wound; Other: standard of care; apply non adherent dressing; Other Names: adaptic

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
time to wound closure	The endpoint of this data collection process is to study the timepoint for total wound closure following the protocol procedures in the use of ProgenaMatrix™.	12 weeks of treatment

Collaborators and Investigators

• Sponsor: ProgenaCare Global, LLC

Study record dates

Study Major Dates

• Study Start (Actual): March 14, 2022
• Primary Completion (Estimated): March 1, 2026
• Study Completion (Estimated): September 1, 2026

Study Registration Dates

• First Submitted: February 22, 2024
• First Submitted That Met QC Criteria: March 1, 2024
• First Posted (Estimated): March 4, 2024

Study Record Updates

• Last Update Posted (Estimated): March 4, 2024
• Last Update Submitted That Met QC Criteria: March 1, 2024
• Last Verified: March 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Cardiovascular Diseases; Vascular Diseases; Skin Diseases; Endocrine System Diseases; Diabetic Angiopathies; Leg Ulcer; Skin Ulcer; Diabetes Complications; Diabetes Mellitus; Diabetic Neuropathies; Foot Diseases; Diabetic Foot; Foot Ulcer
• Other Study ID Numbers: DFU/1

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: Yes
• product manufactured in and exported from the U.S.: No