A Prospective, Multi Centre, Interventional, Non-comparator, Open Label Study to Demonstrate the Efficacy, Performance and Safety of ConvaFoam™ Silicone, ConvaFoam™ Border and ConvaFoam™ Non-Adhesive Dressings in the Management of Surgical and Traumatic Wounds

A prospective, multi centre, interventional, non-comparator, open label study to demonstrate the efficacy, performance and safety of ConvaFoam™ Silicone, ConvaFoam™ Border and ConvaFoam™ Non-Adhesive dressings in the management of surgical and traumatic wounds

Inclusion Criteria:Patients aged 18 years and overPatients able and willing to provide informed consentPatients with Surgical wounds including incisional wounds including laparoscopicwounds and surgical wounds healing by secondary intention.Patients with Traumatic woundsPatients must be willing to attend visits as per schedule in protocolExclusion criteria:Patients with known allergies to any of the materials used in the dressingPatients who require any oxidising agents such as hydrogen peroxide or hypochlorite solutions.Patients, who in the opinion of the investigator, is considered unsuitable for any other reasonPatients with wounds showing signs of infection on presentation or not resolving with the use of antibiotics