Clareo Health | 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
Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
ConvaTec Inc.
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 for up to 4 weeks
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients aged 18 years and over
Patients able and willing to provide informed consent
Patients with Surgical wounds including incisional wounds including laparoscopic
wounds and surgical wounds healing by secondary intention.
Patients with Traumatic wounds
Patients must be willing to attend visits as per schedule in protocol
You may not be if
Patients with known allergies to any of the materials used in the dressing
Patients 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 reason
Patients with wounds showing signs of infection on presentation or not resolving with the use of antibiotics
