Clinical Research Directory

Inclusion Criteria: * Males or females aged 18 years or above. * Patients who can understand and give informed consent to take part in the study. * Have one or more of the following wounds: Diabetic ulcers, Arterial and Venous Leg ulcers, Pressure ulcers, Postoperative wounds healing by secondary intention, traumatic and surgical wounds, and burns and scalds * Wounds that require debridement due to the presence of slough debris/fibrous tissue ,hyperkeratotic debris and dried exudate on the peri wound skin. * Wounds with both serous crusts and healthy tissue. * Minimum of 30% of the wound covered by debris, necrosis or slough. * Wound Size \> 4cm2 Exclusion Criteria: * Patients who are known to be non-compliant with medical treatment * Patients who are known to be sensitive to any of the device components such as polyester. * Subject has any significant or unstable medical or psychiatric condition that, in the opinion of the Investigator, would interfere with their ability to participate in the study. * Subject is currently enrolled in another clinical study, or has completed a clinical study less than 30 days prior to enrolment. * Symptoms \& signs of systemic and / or spreading wound infection (including erythema and fever). * Severe pain (level 7 or higher on a 0-10 VAS or hyperaesthesia in the wound area). * Subjects who in the view of the investigator might not be suitable for inclusion in the study