A Prospective, Randomized, Multicenter, Controlled Evaluation of the Use of Dehydrated Amniotic Membrane Allograft Compared to Standard of Care for the Closure of Chronic Diabetic Foot Ulcers

被引:4
作者
Snyder, Robert J. [1 ]
Shimozaki, Kenneth [2 ]
Tallis, Arthur [3 ]
Kerzner, Michael [4 ]
Reyzelman, Alexander [5 ]
Lintzeris, Dimitrios [6 ]
Bell, Desmond [7 ]
Rutan, Randi L. [8 ]
Rosenblum, Barry [9 ]
机构
[1] Barry Univ Clin Res, 16800 NW 2nd Ave,Suite 202, North Miami Beach, FL 33169 USA
[2] Pacific Wound Ctr, Stockton, CA USA
[3] Associated Foot & Ankle Specialists, Phoenix, AZ USA
[4] Duke Univ, Med Ctr, Durham, NC USA
[5] Clin Res Ctr, San Francisco, CA USA
[6] Wayne Mem Wound Healing & Hyperbar Ctr, Goldsboro, NC USA
[7] First Coast Cardiovasc Inst, Jacksonville, FL USA
[8] Derma Sci Inc, Princeton, NJ USA
[9] Beth Israel Deaconess Med Ctr, Plymouth, MA USA
来源
WOUNDS-A COMPENDIUM OF CLINICAL RESEARCH AND PRACTICE | 2016年 / 28卷 / 03期
关键词
diabetic foot ulcer; dehydrated amniotic membrane allograft; wound closure; MANAGEMENT; PREDICTOR; TRIAL;
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Delayed closure of foot ulcers is a primary factor leading to lower extremity amputation in patients with diabetes, creating great demand for products or therapies to accelerate the rate of wound closure in this population. This study (ClinicalTrials.gov Identifier: NCT02209051) was designed to evaluate dehydrated amniotic membrane allograft (DAMA) (AMNIOEXCEL, Derma Sciences Inc, Princeton, NJ) plus standard of care (SOC) compared to SOC alone for the closure of chronic diabetic foot ulcers (DFUs). Materials and Methods. This prospective, open-label, randomized, parallel group trial was implemented at 8 clinical sites in the United States. Eligibility criteria included adults with type 1 or type 2 diabetes mellitus who have 1 or more ulcers with a Wagner classification of grade 1 or superficial 2 measuring between 1 cm(2) and 25 cm(2) in area, presenting for more than 1 month with no signs of infection/osteomyelitis; ABI > 0.7; HbA1c < 12%; and serum creatinine < 3.0 mg/dL. Eligible subjects were randomized (1:1) to receive either SOC alone (n = 14) or DAMA+SOC (n = 15) until wound closure or 6 weeks, whichever occurred first. The endpoint was the proportion of subjects with complete wound closure (defined as complete reepithelialization without drainage or need for dressings). Results. Thirty-five percent of subjects in the DAMA+SOC cohort achieved complete wound closure at or before week 6, compared with 0% of the SOC alone cohort (intent-to-treat population, P = 0.017). There was a more robust response noted in the per protocol population, with 45.5% of subjects in the DAMA+SOC cohort achieving complete wound closure, while 0% of SOC-alone subjects achieved complete closure (P = 0.0083). No treatment-related adverse events were reported. Conclusion. The results suggest DAMA is safe and effective in the management of DFUs, but additional research is needed.
引用
收藏
页码:70 / 77
页数:8
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