Testing EscharEx against a placebo for venous leg ulcer (VLU)

Exclusion

• −History of allergy or atopic disease or a known sensitivity to pineapples, bromelain, papaya or papain, as well as known sensitivity to latex proteins (known as latex-fruit syndrome), bee venom or olive tree pollen,
• −Wound size that has decreased by \> 20% after 7 (+3/-1) days of the screening periodScreeningThe checks done before joining, to see whether a study fits.Read more →,
• −Patients with more than one leg ulcer, on the leg of the target wound, with an area greater than or equal to 2 cm2, that are between 2cm and 5cm away from the edge of the target wound,
• −Signs of clinical infection of the wound or peri-wound, including purulent discharge, deep-tissue abscess, erysipelas, cellulitis, etc.,
• −Severely damaged skin (e.g. abrasion, erosion, exfoliation) extending \>2 cm around the wound's edge,
• −Presence of gangrene, signs of systemic infection, sepsis, or osteomyelitis during screening phase,
• −Clinical suspicion of skin cancer (e.g., basal cell carcinoma (BCC), squamous cell carcinoma (SCC), melanoma, or sarcoma), near the target wound, which was not ruled out by biopsy,
• −Patients with skin disorders unrelated to the wound that are presented adjacent to the wound,
• −Patients suffering from chronic skin disorders (Idiopathic Pruritus, Psoriasis, Panniculitis, Pyoderma gangrenosum, etc.) that might deteriorate as a result of local trauma or debridement,
• −Wound has sinus tracts or tunnels extending under healthy tissue or penetrating into periosteum, fascia or bone,
• −Patients with primary lymphatic edema (Lymphedema),
• −A significant decrease in the arterial blood flow of the extremity, as demonstrated by either Toe-Brachial Index (TBI) ≤ 0.50, Ankle-Brachial Index (ABI) ≤ 0.70, Skin Perfusion Pressure (SPP) ≤ 40 mmHg, Transcutaneous oximetry (TCOM) ≤ 40 mmHg, or lack of bi-phasic or tri-phasic doppler wave forms,
• −Patients with pre-enrollmentEnrolmentThe number of participants a study plans to include, or has included.Read more → wounds which are covered by eschar heavily saturated with iodine or by silver sulfadiazine (SSD) pseudoeschar (i.e., pseudoeschar as a result of SSD treatment),
• −Patients with poor nutritional status: albumin \< 2.5 g/dl; poorly controlled diabetes mellitus (HbA1c \> 12%); anemia (hemoglobin\<8 g/dL), leukocyte count \< 3,000/μl or \>15000/μl; neutrophil count ≤1000/μl; platelets \<100,000/μl, abnormal liver function (AST, ALT\>2 x upper limit of normal range), renal failure (Cr \> 2.5 mg/dl or eGFR \< 30ml/min /1.73m2), BMI\>48,
• −INR\>2 or PTT \> x 2 ULN (unless the patient receives coumarin derivatives anticoagulants (e.g. warfarin), and the INR and PTT levels are in their required levels and are stable),
• −Patients undergoing renal or peritoneal dialysis,
• −Any condition that would preclude safe participation in the study, e.g., significant or unstable cardiac, vascular, pulmonary, liver, hematological, immunological, neoplastic disease, active COVID-19 or any immediate life-threatening condition,
• −Recent history or concurrent acute injury or disease that might compromise the patient's welfare, according to investigatorPrincipal investigatorThe doctor or researcher responsible for running the study at a site.Read more → discretion,
• −Patients treated with Pentoxifylline within 2 weeks prior to screening,
• −Venous ablation performed within the past month in an area adjacent to the target wound,
• −Mentally incapacitated incompetent adults who are incapable of giving legal consentInformed consentThe process of being told what taking part involves, then choosing freely.Read more → (e.g., dementia, psychiatric patients, etc.),
• −Concurrent use of non-approved drugs or alcohol abuse,
• −Exposure to investigational intervention within one month prior to enrollment, or anticipated participation in another investigational drug trial or other intervention trial, while enrolled in the study.
• −Pregnant women (positive pregnancy test) or nursing mothers,
• −The patient is currently receiving, has received within three months prior to enrollment, or is planned to receive during trial period, any medications or treatments at doses known to impair the wound healing processes. These include chronic systemic steroid intake5 associated with topical skin changes (i.e. thin, fragile skin with multiple hematomas or a history of laceration), immuno-suppressive drugs, immunomodulating medications, chemotherapy, and radiation therapy. Low and intermittent doses that the investigator determines as not clinically significant for wound healing, may be permitted, provided that this determination is based on appropriate clinical judgment and is documented accordingly,