DPP IV Inhibition Facilitates Healing of Chronic Foot Ulcers in Type 2 Diabetes
Chronic Foot Ulcers
About this trial
This is an interventional treatment trial for Chronic Foot Ulcers focused on measuring type 2 diabetes, healing, foot ulcers, vildagliptin
Eligibility Criteria
Inclusion Criteria:
- Type 2 diabetes
- Oral hypoglycemic agents treatment
- Chronic foot ulcers
- Adequate blood circulation (perfusion) was assessed by a dorsum transcutaneous oxygen test >30 -mmHg, anklebrachial index values > 0.7 and < 1.2 with toe pressure > 30 mmHg, or Doppler arterial aveforms that were triphasic or biphasic at the ankle of the affected leg
- Written consensus
Exclusion Criteria:
- Active Charcot disease
- Ulcers resulting from electrical, chemical, or radiation burns
- Collagen vascular disease
- Ulcer malignancy
- Untreated osteomyelitis, or cellulitis
- Ulcer treatment with normothermic or hyperbaric oxygen therapy
- Concomitant medications such as corticosteroids, immunosuppressive medications, or -chemotherapy
- Recombinant or autologous growth factor products
- Skin and dermal substitutes within 30 days of study start
- Use of any enzymatic debridement treatments
- Pregnant or nursing mothers
Sites / Locations
- Second university of Naples
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
Placebo
Vildagliptin
In the placebo group, the dose of other concomitant hypoglycemic medication was changed to obtain a similar profile of metabolic parameters. All patients had diabetes and at least one full-thickness wound below the ankle for >3 months. All patients were examined weekly for the first 4 weeks (day 28) then every other week until day 120 or ulcer closure by any means. At each visit, tracings of the wound margins were made for computer planimetry to document changes in wound size, and photographs were taken for a visual record. All patients followed the regular treatment at the multidisciplinary diabetes foot clinic, included treatment of infection, debridement, off-loading, and metabolic control according to high international standards and standard good medical practice.
The experimental arm followed the same treatment of placebo group, but received also vildagliptin 50 mg per os b.i.d. for 4 months