A purified reconstituted bilayer matrix shows improved outcomes in treatment of non‐healing diabetic foot ulcers when compared to the standard of care: Final results and analysis of a prospective, randomized, controlled, multi‐centre clinical trial

Author:

Armstrong David G.1ORCID,Orgill Dennis P.2ORCID,Galiano Robert D.3ORCID,Glat Paul M.4ORCID,Kaufman Jarrod P.5ORCID,Carter Marissa J.6ORCID,DiDomenico Lawrence A.7,Zelen Charles M.8ORCID

Affiliation:

1. Division of Surgery, Keck School of Medicine University of Southern California Los Angeles California USA

2. Division of Plastic Surgery Brigham and Women's Hospital Boston Massachusetts USA

3. Division of Plastic Surgery, Feinberg School of Medicine Northwestern University Chicago Illinois USA

4. Surgery and Pediatrics Drexel University College of Medicine, St. Christopher's Hospital for Children Philadelphia Pennsylvania USA

5. Department of Surgery, Temple University School of Medicine and McGowan Institute for Regenerative Medicine University of Pittsburgh Pittsburgh Pennsylvania USA

6. Strategic Solutions, Inc. Bozeman Montana USA

7. Lower Extremity Institute for Research and Therapy Youngstown Ohio USA

8. Professional Education and Research Institute Roanoke Virginia USA

Abstract

AbstractAs the incidence of diabetic foot ulcers (DFU) increases, better treatments that improve healing should reduce complications of these ulcers including infections and amputations. We conducted a randomized controlled trial comparing outcomes between a novel purified reconstituted bilayer membrane (PRBM) to the standard of care (SOC) in the treatment of non‐healing DFUs. This study included 105 patients who were randomized to either of two treatment groups (n = 54 PRBM; n = 51 SOC) in the intent to treat (ITT) group and 80 who completed the study per protocol (PP) (n = 47 PRBM; n = 33 SOC). The primary endpoint was the percentage of wounds closed after 12 weeks. Secondary outcomes included percent area reduction, time to healing, quality of life, and cost to closure. The DFUs that had been treated with PRBM healed at a higher rate than those treated with SOC (ITT: 83% vs. 45%, p = 0.00004, PP: 92% vs. 67%, p = 0.005). Wounds treated with PRBM also healed significantly faster than those treated with SOC with a mean of 42 versus 62 days for SOC (p = 0.00074) and achieved a mean wound area reduction within 12 weeks of 94% versus 51% for SOC (p = 0.0023). There were no adverse events or serious adverse events that were related to either the PRBM or the SOC. In comparison to the SOC, DFUs healed faster when treated with PRBM. Thus, the use of this PRBM is an effective option for the treatment of chronic DFUs.

Funder

Geistlich Pharma

Publisher

Wiley

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