Topical PluroGel N for the Treatment of Mildly Infected Diabetic Foot Ulcers

Exclusion Criteria

• •Subjects with IDSA-defined moderate infection as per Appendix C, including cellulitis extending \> 2 cm; lymphangitis; spread beneath the fascia; deep tissue abscess; osteomyelitis; gangrene; muscle, joint, or bone involvement.
• •* Subjects with IDSA-defined severe infection as per Appendix C, within PGN1300 Protocol including systemic toxicity or metabolic instability (e.g., fever, chills, tachycardia, hypotension, confusion, vomiting, leukocytosis, acidosis, hyperglycemia, or azotemia).
• •* Subjects with systemic inflammatory response signs, as manifested by ≥2 of the following :
• •Temperature \>38°C or \<36°C
• •Heart rate \>90 beats/min
• •Respiratory rate \>20 breaths/min or PaCO2 \<32 mm Hg
• •White blood cell count \>12 000 or \<4000 cells/μL or ≥10% immature (band) forms
• •* Subjects with local wound complications (e.g., prosthetic materials).
• •* Subjects currently receiving antibiotic treatment for a localized infection of the study ulcer and whose infection is improving in response to treatment.
• •* Subjects requiring concurrent systemic antimicrobials during the study period for any infection, including diabetic foot ulcer.
• •* Subjects in whom bone or joint involvement is suspected based on clinical examination (e.g., bone noted visually or by probing) or plain view X-ray.
• •* Subjects with clinically significant peripheral arterial disease requiring vascular reconstructive surgery. Subjects who are expected to be unable to care for their ulcer because of hospitalization, vacation, disability, etc. during the study period, or are unable to safely monitor the infection status at home.
• •* Subjects with known active alcohol or substance abuse within the 6 months preceding study entry.
• •* Subjects who are receiving immunosuppressive agents (other than corticosteroids), radiation therapy, or cytotoxic agents.
• •* Subjects who require treatment for a primary or metastatic malignancy (other than squamous or basal cell carcinoma of the skin).
• •* Subjects with a systemically immunocompromising disease, such as acquired immune deficiency syndrome or known human immunodeficiency virus infection.
• •* Subjects who have had an unexplained fever or chills during the week prior to enrollment.
• •* Subjects with other conditions considered by the investigator to be reasons for disqualification that may jeopardize subject safety or interfere with the objectives of the trial (e.g., acute illness or exacerbation of chronic illness, lack of motivation, history of poor compliance).
• •* Subjects with any known allergy or other contraindication to any ingredients in the study products.
• •* Women who are breast feeding, pregnant, or not using contraception unless sterile.
• •* Subjects who have been taking or expect to be taking any other investigational therapy within the 30 days prior to entry or during enrollment.