Efficacy of ProgenaMatrix™ in the Management of DFUs

NCT ID: NCT06292026

Last Updated: 2024-03-04

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-03-14
• Study Completion Date: 2026-09-30

Brief Summary

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

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.

Conditions

Diabetic Foot Ulcer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment with ProgenaMatrix

application of ProgenaMatrix daily for 12 weeks

Group Type: EXPERIMENTAL

ProgenaMatrix Keratin graft

Intervention Type: DEVICE

place ProgenaMatrix graft on the wound

standard of care

Intervention Type: OTHER

apply non adherent dressing

Interventions

ProgenaMatrix Keratin graft

place ProgenaMatrix graft on the wound

Intervention Type: DEVICE

standard of care

apply non adherent dressing

Intervention Type: OTHER

Other Intervention Names

adaptic

Eligibility Criteria

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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

ProgenaCare Global, LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

United Wound Healing

Puyallup, Washington, United States

Countries

United States

Other Identifiers

DFU/1

Identifier Type: -

Identifier Source: org_study_id