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An open-label trial of cryopreserved human umbilical cord in the treatment of complex diabetic foot ulcers complicated by osteomyelitis.
Marston, William A; Lantis, John C; Wu, Stephanie C; Nouvong, Aksone; Lee, Tommy D; McCoy, Nicholas D; Slade, Herbert B; Tseng, Scheffer C.
Affiliation
  • Marston WA; Division of Vascular Surgery, University of North Carolina School of Medicine, Chapel Hill, North Carolina.
  • Lantis JC; Department of Surgery, Mt Sinai West and St Luke's Hospitals, New York, New York.
  • Wu SC; Department of Podiatric Surgery & Applied Biomechanics, Rosalind Franklin University, North Chicago, Illinois.
  • Nouvong A; Department of Surgery, UCLA, Los Angeles, California.
  • Lee TD; Research & Development, TissueTech, Inc., Miami, Florida.
  • McCoy ND; Research & Development, TissueTech, Inc., Miami, Florida.
  • Slade HB; Research & Development, TissueTech, Inc., Miami, Florida.
  • Tseng SC; Department of Pediatrics, University of North Texas Health Sciences Center, Fort Worth, Texas.
Wound Repair Regen ; 27(6): 680-686, 2019 11.
Article in En | MEDLINE | ID: mdl-31376297
ABSTRACT
Clinical trials of potential new therapies for diabetic foot ulcers rarely enroll patients whose wounds extend to muscle, fascia, or bone with clinical and radiographic evidence of underlying osteomyelitis. An open-label, multicenter trial of cryopreserved human umbilical cord (TTAX01) was undertaken in 32 subjects presenting with such complex wounds with a mean duration of 6.1 ± 9.0 (range 0.2-47.1) months and wound area at screening of 3.8 ± 2.9 (range 1.0-9.6) cm2 . Aggressive surgical debridement at baseline resulted in 17 minor amputations and an increase in mean wound area to 7.4 ± 5.8 (range 1.1-28.6) cm2 . All subjects were placed on systemic antibiotics for at least 6 weeks in conjunction with baseline application of TTAX01. Repeat applications were made at no less than 4-week intervals over the 16-week trial. Initial closure occurred in 18 of 32 (56%) wounds, with 16 (50%) of these having confirmed closure in 16 weeks with a median of one-product application. Cases with biopsy confirmed osteomyelitis (n = 20) showed initial closure in 12 (60%) wounds and confirmed closure in 10 (50%) wounds. Four of the five ulcers presenting as recurrences experienced confirmed closure. Mean overall time to healing was 12.8 ± 4.3 weeks. Mean wound area reduction from baseline was 91% for all wounds. Of the 16 wounds without confirmed closure during the 16-week treatment period, five (31.3%) achieved 99-100% wound area reduction by their final visit. The product was well tolerated. Two minor amputations occurred during the study period due to recurrent or persistent osteomyelitis; however, there were no major amputations.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteomyelitis / Umbilical Cord / Wound Healing / Diabetic Foot / Diabetes Mellitus, Type 2 Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Wound Repair Regen Journal subject: DERMATOLOGIA Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteomyelitis / Umbilical Cord / Wound Healing / Diabetic Foot / Diabetes Mellitus, Type 2 Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Wound Repair Regen Journal subject: DERMATOLOGIA Year: 2019 Document type: Article