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Published on: August 4, 2017
Promotion and acceleration of diabetic ulcer healing by arginine-glycine-aspartic acid (RGD) peptide matrix. RGD
D L Steed1, J J Ricotta, J J Prendergast
1Department of Surgery, University of Pittsburg, Pennsylvania 15213.
Diabetes Care
|January 1, 1995
Summary
Arginine-glycine-aspartic acid (RGD) peptide matrix significantly improved healing rates for diabetic foot ulcers. This treatment promoted faster and more complete ulcer closure compared to placebo.
Area of Science:
- Wound healing research
- Diabetic complications
- Biomaterials in medicine
Background:
- Diabetic foot ulcers represent a significant clinical challenge with high morbidity.
- Current treatments for chronic diabetic foot ulcers have limited efficacy.
- Novel therapeutic strategies are needed to accelerate wound closure.
Purpose of the Study:
- To evaluate the efficacy and safety of arginine-glycine-aspartic acid (RGD) peptide matrix for treating diabetic foot ulcers.
- To compare RGD peptide matrix treatment with placebo in a randomized controlled trial.
Main Methods:
- A prospective, multicenter, randomized, placebo-controlled, double-blind study.
- Sixty-five patients with chronic full-thickness neurotrophic diabetic foot ulcers were enrolled.
- Topical application of RGD peptide matrix or placebo twice weekly for up to 10 weeks.
Main Results:
- Complete ulcer healing occurred in 35% of patients treated with RGD peptide matrix versus 8% in the placebo group (P=0.02).
- Over 50% ulcer closure was achieved by 75% of RGD peptide matrix patients compared to 48% of placebo patients (P=0.03).
- RGD peptide matrix significantly accelerated the rate of ulcer closure over 10 weeks (P=0.03).
Conclusions:
- RGD peptide matrix treatment significantly promotes and accelerates the healing of chronic diabetic foot ulcers.
- The findings support the use of RGD peptide matrix as an effective therapeutic option for diabetic foot ulcers.

