{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T06:44:04Z","timestamp":1790837044516,"version":"4.1.0"},"reference-count":37,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2015,10,19]],"date-time":"2015-10-19T00:00:00Z","timestamp":1445212800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Integra LifeSciences Corporation"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Wound Repair Regeneration"],"published-print":{"date-parts":[[2015,11,12]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    Individuals with diabetes mellitus are at an increased risk of developing a diabetic foot ulcer (DFU). This study evaluated the safety and efficacy of Integra Dermal Regeneration Template (IDRT) for the treatment of nonhealing DFUs. The Foot Ulcer New Dermal Replacement Study was a multicenter, randomized, controlled, parallel group clinical trial conducted under an Investigational Device Exemption. Thirty\u2010two sites enrolled and randomized 307 subjects with at least one DFU. Consented patients were entered into the 14\u2010day run\u2010in phase where they were treated with the standard of care (0.9% sodium chloride gel) plus a secondary dressing and an offloading\/protective device. Patients with less than 30% reepithelialization of the study ulcer after the run\u2010in phase were randomized into the treatment phase. The subjects were randomized to the control treatment group (0.9% sodium chloride gel;\n                    <jats:italic>n<\/jats:italic>\n                    \u2009=\u2009153) or the active treatment group (IDRT,\n                    <jats:italic>n<\/jats:italic>\n                    \u2009=\u2009154). The treatment phase was 16 weeks or until confirmation of complete wound closure (100% reepithelialization of the wound surface), whichever occurred first. Following the treatment phase, all subjects were followed for 12 weeks. Complete DFU closure during the treatment phase was significantly greater with IDRT treatment (51%) than control treatment (32%;\n                    <jats:italic>p<\/jats:italic>\n                    \u2009=\u20090.001) at sixteen weeks. The median time to complete DFU closure was 43 days for IDRT subjects and 78 days for control subjects in wounds that healed. The rate of wound size reduction was 7.2% per week for IDRT subjects vs. 4.8% per week for control subjects (\n                    <jats:italic>p<\/jats:italic>\n                    \u2009=\u20090.012). For the treatment of chronic DFUs, IDRT treatment decreased the time to complete wound closure, increased the rate of wound closure, improved components of quality of life and had less adverse events compared with the standard of care treatment. IDRT could greatly enhance the treatment of nonhealing DFUs.\n                  <\/jats:p>","DOI":"10.1111\/wrr.12357","type":"journal-article","created":{"date-parts":[[2015,8,22]],"date-time":"2015-08-22T09:42:11Z","timestamp":1440236531000},"page":"891-900","source":"Crossref","is-referenced-by-count":238,"title":["A clinical trial of Integra Template for diabetic foot ulcer treatment"],"prefix":"10.1111","volume":"23","author":[{"given":"Vickie R.","family":"Driver","sequence":"first","affiliation":[{"name":"Department of Orthopedic Surgery (Clinical) Brown University Alpert School of Medicine Providence Rhode Island"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lawrence A.","family":"Lavery","sequence":"additional","affiliation":[{"name":"Department of Plastic Surgery University of Texas Southwestern Dallas Texas"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alexander M.","family":"Reyzelman","sequence":"additional","affiliation":[{"name":"Department of Medicine, California School of Podiatric Medicine and UCSF Center for Limb Preservation California School of Podiatric Medicine at Samuel Merritt University Oakland California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Timothy G.","family":"Dutra","sequence":"additional","affiliation":[{"name":"Applied Biomechanics California School of Podiatric Medicine at Samuel Merritt University Oakland California"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cyaandi R.","family":"Dove","sequence":"additional","affiliation":[{"name":"Advanced Foot &amp; Ankle Center Las Vegas Nevada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sandra V.","family":"Kotsis","sequence":"additional","affiliation":[{"name":"Section of Plastic Surgery, Department of Surgery The University of Michigan Medical School"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hyungjin Myra","family":"Kim","sequence":"additional","affiliation":[{"name":"Center for Statistical Consultation and Research The University of Michigan Ann Arbor Michigan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kevin C.","family":"Chung","sequence":"additional","affiliation":[{"name":"Section of Plastic Surgery, Department of Surgery The University of Michigan Medical School"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2015,10,19]]},"reference":[{"key":"e_1_2_9_2_1","volume-title":"Diabetic foot and ulceration: epidemiology and pathophysiology","author":"Boulton A","year":"2005"},{"key":"e_1_2_9_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.mpmed.2010.08.011"},{"issue":"4","key":"e_1_2_9_4_1","first-page":"S1","article-title":"Consensus recommendations on advancing the standard of care for treating neuropathic foot ulcers in patients with diabetes","volume":"56","author":"Snyder RJ","year":"2010","journal-title":"Ostomy Wound Manage"},{"key":"e_1_2_9_5_1","doi-asserted-by":"publisher","DOI":"10.2337\/diacare.22.5.692"},{"key":"e_1_2_9_6_1","doi-asserted-by":"publisher","DOI":"10.2337\/dc05-2425"},{"key":"e_1_2_9_7_1","doi-asserted-by":"publisher","DOI":"10.2337\/diacare.22.3.382"},{"key":"e_1_2_9_8_1","doi-asserted-by":"publisher","DOI":"10.7547\/87507315-84-7-322"},{"key":"e_1_2_9_9_1","doi-asserted-by":"publisher","DOI":"10.2337\/diacare.12.1.24"},{"key":"e_1_2_9_10_1","doi-asserted-by":"publisher","DOI":"10.2337\/dc13-2176"},{"key":"e_1_2_9_11_1","doi-asserted-by":"publisher","DOI":"10.1053\/j.jfas.2008.02.015"},{"key":"e_1_2_9_12_1","doi-asserted-by":"publisher","DOI":"10.1007\/s11136-006-0031-y"},{"key":"e_1_2_9_13_1","doi-asserted-by":"publisher","DOI":"10.1177\/107110070602700408"},{"key":"e_1_2_9_14_1","unstructured":"The University of Michigan Medical School The University of Michigan Health System's Educational Services for Nursing Barry University School of Podiatric Medicine. The standard of care for evaluation and treatment of diabetic foot ulcers.2010. Available athttp:\/\/www.woundcarenurses.org\/uploads\/7\/6\/6\/7\/7667574\/diabetic_ulcers.pdf(accessed May 29 2014)."},{"key":"e_1_2_9_15_1","doi-asserted-by":"publisher","DOI":"10.2337\/diacare.24.2.290"},{"key":"e_1_2_9_16_1","doi-asserted-by":"publisher","DOI":"10.2337\/diacare.26.6.1701"},{"key":"e_1_2_9_17_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1742-481X.2009.00585.x"},{"key":"e_1_2_9_18_1","doi-asserted-by":"publisher","DOI":"10.1111\/iwj.12329"},{"key":"e_1_2_9_19_1","doi-asserted-by":"publisher","DOI":"10.1002\/jbm.820140108"},{"key":"e_1_2_9_20_1","doi-asserted-by":"publisher","DOI":"10.1097\/00004630-200301000-00009"},{"key":"e_1_2_9_21_1","unstructured":"U.S. Department of Health & Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for Biologics Evaluation and Research (CBER) Center for Devices and Radiological Health (CDRH). 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