Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers

Not Applicable

Completed

Brief Summary: Have indolent diabetic ulcers completely healed by the Acellular Porcine Dermal Matrix (APM) in 12 weeks.

Detailed Description: The primary objective of this study is time -to - healing with wound size determination at 12 weeks.

Recruitment & Eligibility

Inclusion Criteria

Inclusion Criteria and Population:

Male or female age 18 or older
Informed consent must be obtained
Patient's ulcer must be diabetic in origin and larger than 1cm2. Debridement will be done prior to randomization. Subject's informed consent for participating in this study, must be obtained prior to proceeding with sharp debridement.
Patients with Type 1 or Type 2 diabetes (criteria for the diagnosis of diabetes mellitus per ADA).
Patient's ulcer must exhibit no clinical signs of infection.
Patient is of legal consenting age.
Patient is willing to provide informed consent and is willing to participate in all procedures and follow up evaluations necessary to complete the study.
Patient has adequate circulation to the affected extremity, as demonstrated by one of the following within the past 60 days:
- Dorsum transcutaneous oxygen test (TcPO2) with results ≥30mmHg, OR
- ABIs with results of ≥0.7 and ≤1.2, OR
- Doppler arterial waveforms,which are triphasicor biphasic at the ankle of affected leg

Exclusion Criteria

Patients presenting with an ulcer probing to bone (UT Grade IIIA-D). A positive probe-to-bone will be confirmed when bone or joint can be felt with a sterile, ophthalmological probe.
Patients whose index diabetic foot ulcers are greater than 25cm2.
Patients considered not in reasonable metabolic control, confirmed by an HgA1c greater than 12% within previous 90 days,
Patients whose serum creatinine levels are 3.0mg/dl or greater.
Patients with a known history of poor compliance with medical treatments.
Patients who have been previously randomized into this study, or are presently participating in another clinical trial
Patients who are currently receiving radiation therapy or chemotherapy.
Patients with known or suspected local skin malignancy to the index diabetic ulcer.
Patients on anticoagulant medication will as in any surgical procedure, be monitored According to the protocols employed at the enrolling center.
Patients diagnosed with autoimmune connective tissues diseases.
Nonrevascularable surgical sites
Active infection at site
Sensitivity to the following antibiotics: Gentamicin, Cefoxilin, Linocmycin, Polymyxin B, Vancomycin
Any pathology that would limit the blood supply and compromise healing;
Patients that have received a biomedical or topical growth factor for their wound within the previous 30 days

Arm && Interventions

Group	Intervention	Description
APM Graft (BIOTAPE XMTM	APM Graft (BIOTAPE XMTM)	graft applied to wound q 3 weeks for 12 weeks
standard wound care	Wound Debridement	Wound debridement and gels and foams applied to wound weekly for 12 weeks.
APM Graft (BIOTAPE XMTM	Wound Debridement	graft applied to wound q 3 weeks for 12 weeks

Primary Outcome Measures

Name	Time	Method
Size of Index Wound Based on Calculations Wound Width x Length x Depth 2. Size of Index Wound Based on Calculations Wound Width x Length x Depth	12 Weeks	Wound evaluated and granulation described by wound tracing and photographs which will be measures in wound width x length x depth at each week for 12 weeks or until full granulation has occurred in addition to the size of the wound

Secondary Outcome Measures

Name	Time	Method

Locations (2): Professional Education & Research Institute
🇺🇸
Roanoke, Virginia, United States
Advanced Foot Care and Clinincal Research Center
🇺🇸
Fresno, California, United States