NCT05632276View on ClinicalTrials.gov

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

NACompletedINTERVENTIONAL
Enrollment

54

Participants

Timeline

Start Date

June 8, 2023

Primary Completion Date

March 13, 2024

Study Completion Date

March 13, 2024

Conditions
Surgical WoundTrauma-related Wound
Interventions
DEVICE

ConvaFoam

ConvaFoam™ Border, ConvaFoam™ Non-Adhesive, and ConvaFoam™ Silicone dressings are designed to provide a moist wound healing environment. All participants will be assigned a dressing based upon clinical judgement for a maximum of 4 weeks with weekly assessments and dressing changes

Trial Locations (2)

27157

Wake Forest School of Medicine, Winston-Salem

02218

Boston Medical Center, Boston

Sponsors

Lead Sponsor

ConvaTec Inc.
All Listed Sponsors
lead

ConvaTec Inc.

INDUSTRY

NCT05632276 - 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 | Biotech Hunter | Biotech Hunter