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

Primary Purpose

Diabetic Foot Ulcers

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
APM Graft (BIOTAPE XMTM)
Wound Debridement
Sponsored by
Stryker Trauma GmbH
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Foot Ulcers focused on measuring Diabetic Foot Ulcers

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Advanced Foot Care and Clinincal Research Center
  • Professional Education & Research Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

APM Graft (BIOTAPE XMTM

standard wound care

Arm Description

graft applied to wound q 3 weeks for 12 weeks

Wound debridement and gels and foams applied to wound weekly for 12 weeks.

Outcomes

Primary Outcome Measures

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
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

Full Information

First Posted
May 11, 2011
Last Updated
May 18, 2021
Sponsor
Stryker Trauma GmbH
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1. Study Identification

Unique Protocol Identification Number
NCT01353495
Brief Title
Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
Official Title
A Prospective, Randomized Comparative Parallel Study of Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
April 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Stryker Trauma GmbH

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Foot Ulcers
Keywords
Diabetic Foot Ulcers

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
39 (Actual)

8. Arms, Groups, and Interventions

Arm Title
APM Graft (BIOTAPE XMTM
Arm Type
Experimental
Arm Description
graft applied to wound q 3 weeks for 12 weeks
Arm Title
standard wound care
Arm Type
Active Comparator
Arm Description
Wound debridement and gels and foams applied to wound weekly for 12 weeks.
Intervention Type
Device
Intervention Name(s)
APM Graft (BIOTAPE XMTM)
Other Intervention Name(s)
BIOTAPE XMTM
Intervention Description
Patients randomized to the APM group will, following surgical debridement for their diabetic foot wounds, receive a single application of an APM graft (BIOTAPE XMTM, Wright Medical Technology, USA) with dressing changes taking place weekly. All necrotic tissue will be removed from the wound prior to application. BIOTAPE XMTM will be sutured or stapled in place under a silver-based non-adherent dressing (Silverlon, Argenta Medical). Therapy will then be followed by a moisture-retentive dressing (hydrogel bolster) until complete epithelialization has occurred.
Intervention Type
Other
Intervention Name(s)
Wound Debridement
Intervention Description
Wounds debrided in both arms of study
Primary Outcome Measure Information:
Title
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
Description
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
Time Frame
12 Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jagpreet Mukker, DPM
Organizational Affiliation
Advanced Foot Care and Clinincal Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Advanced Foot Care and Clinincal Research Center
City
Fresno
State/Province
California
ZIP/Postal Code
93722
Country
United States
Facility Name
Professional Education & Research Institute
City
Roanoke
State/Province
Virginia
ZIP/Postal Code
24016
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

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

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