RecruitingNot ApplicableNCT07632001

Miro3D Wound Matrix for Treatment of Diabetic Foot Ulcers

A Randomized Controlled Multicenter Trial, Examining the Effect of Miro3D Wound Matrix on the Rate of Complete Wound Closure of Chronic Diabetic Foot Ulcers


Sponsor

Reprise Biomedical, Inc.

Enrollment

180 participants

Start Date

Jun 15, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study is designed to evaluate whether the Miro3D Wound Matrix, when used in addition to standard of care, improves healing outcomes in patients with chronic diabetic foot ulcers. Diabetic foot ulcers are a common and serious complication of diabetes and may be difficult to heal despite appropriate treatment. Standard of care typically includes regular wound cleaning, debridement (removal of dead tissue), offloading (reducing pressure on the wound), and moisture-balancing dressings. However, some wounds fail to heal with standard treatment alone. Miro3D Wound Matrix is a three-dimensional, acellular scaffold derived from porcine tissue that is intended to support wound healing. This study will compare outcomes in patients treated with Miro3D plus standard of care versus standard of care alone. Approximately 180 adult subjects with non-healing diabetic foot ulcers will be enrolled at multiple clinical sites in the United States. After a two-week screening period, eligible participants will be randomly assigned to receive either Miro3D in addition to standard of care or standard of care alone. Subjects will be followed for up to 12 weeks with weekly clinic visits. The primary objective of the study is to determine whether treatment with Miro3D increases the rate of complete wound closure and improves reduction in wound size compared to standard of care alone. Safety will also be evaluated by monitoring adverse events throughout the study.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Miro3D Wound Matrix and Standard of Care for people with chronic wounds, diabetic foot, and other related conditions. The study is currently recruiting participants at 14 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEMiro3D Wound Matrix

Miro3D Wound Matrix is a sterile, acellular, three-dimensional scaffold derived from porcine liver tissue and applied topically to the wound following appropriate wound bed preparation to support tissue regeneration and healing.

OTHERStandard of Care

Standard of care includes sharp debridement, offloading using a protocol-defined device, and appropriate moisture-retentive dressings.


Locations(14)

Advanced Foot Care

Phoenix, Arizona, United States

West Boca Center for Wound Healing

Coconut Creek, Florida, United States

Solutions Medical Research

Coral Gables, Florida, United States

Doctors Research Network

Miami, Florida, United States

Barry University

Tamarac, Florida, United States

Clinical Trials of New England

Hyde Park, Massachusetts, United States

Mercy Hyperbaric and Wound Care

St Louis, Missouri, United States

St. Louis Foot & Ankle

St Louis, Missouri, United States

Christian Hospital Wound Center

St Louis, Missouri, United States

Icahn School of Medicine at Mount Sinai

New York, New York, United States

ABC Podiatry

Columbus, Ohio, United States

Dynamic Wound Care

Oklahoma City, Oklahoma, United States

Caring Foot and Ankle Specialists

Houston, Texas, United States

Vital Heart and Vein

Humble, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07632001


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