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Active, not recruiting Not applicable Interventional

Matrion Decellularized Placental Membrane Versus Conventional Wound Management in Subjects With Diabetic Foot Ulcers

ClinicalTrials.gov ID: NCT07116876

Public ClinicalTrials.gov record NCT07116876. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 11:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label Trial to Assess the Clinical Effectiveness of Matrion Decellularized Placental Membrane Versus Conventional Wound Management in Subjects With Diabetic Foot Ulcers

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will evaluate Matrion™ (LifeNet Health, Inc., Virginia Beach, VA), a placental membrane product, as a treatment for diabetic foot ulcers compared to conventional wound care. Matrion is derived from donated human birth tissue and includes both the amniotic and chorionic layers, along with the trophoblast layer. It is minimally processed using a proprietary decellularization method and terminally sterilized to ensure the membrane is acellular and sterile, making it suitable for surgical applications.

Study identification

NCT ID
NCT07116876
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
LifeNet Health
Industry
Enrollment
120 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 26, 2025 (Actual)
Primary completion
Dec 15, 2026 (Estimated)
Completion
Dec 30, 2026 (Estimated)
Last update posted
Sep 14, 2026

2025 – 2026

United States locations

U.S. sites
17
U.S. states
7
U.S. cities
16
Facility City State ZIP Site status
Compass Medical Research Center Tucson Arizona 85715 —
Bay Area Foot Care Castro Valley California 94546 —
Limb Preservaion Platform, Inc. Fresno California 93710 —
Center for Clinical Research, Inc San Francisco California 94115 —
Bay Area Foot Care San Francisco California 94117 —
ILD Research Center Vista California 92081 —
Humanity Clinical Research, Corp Aventura Florida 33180 —
Dinamo Research & Diagnostic Center, LLC Hialeah Florida 33015 —
Doctors Research Network, Inc. Miami Florida 33156 —
Independent Clinical Research Decatur Illinois 62521 —
Independent Clinical Research, LLC Springfield Illinois 62704 —
US Foot and Ankle Specialists Raleigh North Carolina 27609 —
Foot and Ankle Institute of the Carolinas Rocky Mount North Carolina 27804 —
Olympus Clinical Research Katy Texas 77450 —
Element Research Group San Antonio Texas 78258 —
Olympus-Alcanza Sugar Land Texas 77479 —
Foot and Ankle Specialists of the Mid-Atlantic Salem Virginia 24175 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07116876, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 14, 2026 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07116876 live on ClinicalTrials.gov.

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