Provant Therapy of Venous Stasis Ulcer Trial

Exclusion Criteria

• •No ulcer on the target limb including the study ulcer may be deep enough to expose structures deep to the adipose lay of skin such as muscle, fascia, tendon, joint, or bone. The presence of sinus tracts that have not been sufficiently marsupialized such that the wound depth can be assessed by gross visual inspection is similarly exclusion.
• •At the Screening or Randomization Visits, the presence of significant periwound cellulitis or the need to administer systemic antibiotics. system antibiotic therapy for any indication within 10 days of screening is an exclusion.
• •Baseline arterial studies obtained within one year of screening or at the screening visit must show either an ankle-brachial index of the affected limb greater or equal to 0.75 based on the higher of the two pedal arteries systolic pressure measured with Doppler ultrasound compared to the ipsilateral brachial artery systolic pressure determined with Doppler ultrasound.
• •Any major surgery or trauma affecting the target limb such as tibial fracture, knee arthroplasty, endovascular or open arterial or venous surgery or femoral stenting within 180 days of randomization.
• •Participation in any clinical trial involving therapy for wound healing within 30 days of randomization.
• •Concurrent administration of systemic agents that influence wound healing such as prednisone or dexamethasone in any quantity, cytotoxic chemotherapy agents, or immunosuppressive therapy.
• •Previous ionizing radiation therapy at any dose near the wound bed (within 5 cm).
• •A history of cancer in the target limb except for previous skin cancer treated in the target limb provided that a biopsy of the target wound is obtained within 90 days of randomization that confirms the absence of neoplasia.
• •Severe renal failure - serum creatinine greater than 2.5 or subject on hemodialysis.
• •Severe hepatic insufficiency: known cirrhosis, any degree of ascites, serum transamines more than three times the upper limit of normal.
• •Known allergy or intolerance to cadexomeric iodine or latex free Profore bandages.
• •The presence of 1) implanted pacemaker, automatic defibrillator, neurostimulator, bone stimulators, cochlear implants, or other devices with metal leads; 2) implanted or programmable pumps or intravenous or intrathecal drug delivery; 3) metal implant within 25 cm of area of treatment.
• •Pregnancy. Women of childbearing potential must agree to use adequate contraception.
• •Live expectancy of last than one year.
• •Uncompensated or uncontrolled right heart failure with associated edema.
• •Inability to walk independently (adaptive devices such as walkers or canes are allowed).
• •BMI greater than 50.
• •Severe anemia, hemoglobin less than 8.5
• •Poorly controlled diabetes, A1cHgb greater than 12
• •Severe hypoalbuminemia, serum albumen less than 2.6.
• •Active local or systemic malignancy such as lung cancer or leukemia
• •Severe hypertension - systolic bp greater than 180 or diastolic bp greater than 100
• •Severe hypoxemia - chronic oxygen or ventilator therapy.
• •HIV infection unless on retroviral therapy and viral load undetectable by PCR.