A Clinical Study on New Negative Pressure Wound Therapy Dressing in the Management of Chronic & Acute Wounds

Inclusion Criteria

• •Subject has provided written informed consent.
• •Subject is 18 years of age or over.
• •Subject is able and willing to comply with study requirements.
• •Subject is suitable to participate in the study in the opinion of the Investigator. .
• •Subject has a wound(s) that, per Instructions for Use (IFU), is indicated and suitable for management with NPWT and fits one of the following wound types: a. Chronic\* (this may include Diabetic Foot Ulcers (DFUs), Venous Leg Ulcers (VLUs), Pressure Ulcers but this is not an exhaustive list) b. Acute (this may include traumatic and dehisced surgical wounds and partial thickness burns) \*Chronic wound(s) in this study is defined as any wound of less than three months duration that is not healing after thirty (30) days of standard care and having addressed the underlying cause
• •Subject's wound to be treated is of a size that can be managed with one of the available sizes of the study device
• •Subject has had the target wound for greater than three months.
• •Subject has a target wound that measures \<3 millimeters (mm) in maximum depth.
• •Subject has untreated osteomyelitis
• •Subject has active, untreated soft tissue infection.
• •Subject has wounds that has been managed with NPWT in the previous four (4) weeks
• •Subject has participated previously in this clinical trial.
• •Subject has a history of poor compliance with medical treatment.
• •Pregnancy at time of enrolment.
• •Subject has a medical or physical condition that in the opinion of the Investigator would preclude safe subject participation in the study.