A Safety and Efficacy Study of INTEGRA® Dermal Regeneration Template for the Treatment of Diabetic Foot Ulcers

Integra LifeSciences

Status

Completed

Conditions

Neuropathic Diabetic Ulcer - Foot

Treatments

Other: Conventional Wound Therapy

Device: Integra® Dermal Regeneration Template

Study type

Interventional

Funder types

Industry

Identifiers

NCT01060670

IDRT/DFU US - 2009-3

Details and patient eligibility

About

The objective of this study is to evaluate the safety and efficacy of the INTEGRA® Dermal Regeneration Template for the treatment of diabetic foot ulcers located distal to the malleolus in subjects with diabetes mellitus, neuropathy, and without significantly compromised arterial circulation.

Enrollment

545 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Type I or Type II diabetes mellitus
Glycosylated hemoglobin, HbA1c, ≤ 12%
Negative serum pregnancy test at screening for female participants of child-bearing potential
Willing and able to maintain the required off-loading (as applicable for the location for the ulcer) and applicable dressing changes
At least one DFU that met the following criteria:
1. Ulcer was diagnosed as a full-thickness neuropathic DFU that was located distal to the malleolus (excluding ulcers between the toes but including those of the heel),
2. Minimum 2-cm margin between the qualifying study ulcer and any other ulcers on the specified foot (post debridement),
3. Area greater than or equal to 1 square centimeter and less than or equal to 12 square centimeters (post debridement at the time of randomization),
4. Wagner grade 1 or 2,
5. Depth less than or equal to 5 millimeters with no exposed capsule, tendon or bone and no tunneling, undermining or sinus tracts,
6. Duration of the study ulcer was at least 30 days at the time of the screening visit
Adequate vascular perfusion of the affected limb

Exclusion criteria

Suspected or confirmed signs/symptoms of gangrene or wound infection on any part of the limb
History of hypersensitivity to bovine collagen and/or chondroitin.
Pregnancy
Previous treatment under this clinical protocol
Participation in another clinical trial involving a device or systematically administered investigational study drug or treatment within 30 days of the randomization visit.
Receiving or scheduled to receive a medication or treatment which, in the opinion of the investigator, was known to interfere with, or affect the rate and quality of wound healing
Any unstable condition or circumstance that could interfere with treatment regimen compliance
Excessive lymphedema that could interfere with wound healing
Unstable Charcot foot or Charcot with boney prominence
Ulcers secondary to a disease other than diabetes
Osteomyelitis with necrotic soft bone
Chopart amputation
History of bone cancer or metastatic disease of the affected limb, radiation therapy to the foot, or chemotherapy within the 12 months prior to randomization
Treatment with wound dressings that include growth factors, engineered tissues, or skin substitutes within 30 days of randomization or scheduled to receive such treatment during the study
Non-study ulcer requiring treatment that could not be treated during the study with moist wound therapy
History of or intercurrent illnesses or conditions (other than diabetes) that would compromise the safety of the subject, or the normal wound healing process
Employees or relatives of any member of the investigational site or sponsor
Size of the study ulcer following debridement decreased by more than 30% during the run in period