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Saginaw, Michigan 48602


Purpose:

The purpose of this study is to compare the clinical and economic effectiveness of PriMatrix and Standard of Care in the treatment of diabetic foot ulcers (DFUs) in subjects with controlled diabetes mellitus and without significantly compromised arterial circulation.


Study summary:

Subjects will be considered for screening upon meeting initial eligibility criteria. After a 2 week screening period, subject will be randomized and enrolled if additional criteria is met. In particular, if wound size has decreased by greater than 40%, subject will be considered a screen fail and randomization will not take place. If all criteria including wound size at Week 3 is met, subject will be randomized and enrolled. Subjects will return weekly for a maximum of 12 weeks, or whenever healing occurs and then once more for a confirmation of healing. Week 24 will consist of a phone call to the subject to complete QOL surveys.


Criteria:

Inclusion Criteria: - Men or women ≥ 18 years of age and able to give their own consent - Type I or Type II diabetes with investigator-confirmed reasonable metabolic control - Study ulcer has a Wagner grade of 1 or 2 - Study ulcer size of at least 1 cm2, but not exceeding 20 cm2 in area after debridement - A full thickness diabetic foot ulcer located on the foot or ankle - An ulcer which has been in existence for a minimum of 30 days, prior to the day of screening. Exclusion Criteria: - Suspected or confirmed signs/symptoms of wound infection - Wounds with exposed bone or tendon - Hypersensitivity to bovine collagen


NCT ID:

NCT01270633


Primary Contact:

Study Chair
Yiannis Monovoukas, PhD
TEI


Backup Contact:

N/A


Location Contact:

Saginaw, Michigan 48602
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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