914
Participants
Start Date
January 1, 2026
Primary Completion Date
December 31, 2028
Study Completion Date
December 31, 2030
Permanent Suture
In both control and intervention groups, an open umbilical hernia repair will be performed based on a standardized surgical technique. Dissection and identification of the fascial defect will be performed in a standardized manner. In the control group, a permanent 0-0 polypropylene suture will be used to close the hernia defect in a transverse or vertical interrupted fashion using either the simple interrupted or the figure-of-eight technique. If the surgeon creates an opening in the umbilical skin or extends the skin incision beyond the paraumbilical incision during the procedure, the participant will be excluded from the study.
Absorbable
In both control and intervention groups, an open umbilical hernia repair will be performed based on a standardized surgical technique. Dissection and identification of the fascial defect will be performed. An 0-0 polydioxanone suture (PDS) will be used to close the hernia defect in either a transverse or vertical interrupted fashion using either simple interrupted or figure-of-eight technique. If the surgeon creates an opening in the umbilical skin or extends the skin incision beyond the paraumbilical incision during the procedure, the participant will be excluded from the study.
Royal Alexandra Hospital/University of Alberta, Edmonton
Royal Victoria Hospital, Barrie
London Health Sciences Centre, London
North York General Hospital, North York
Vancouver Coastal Health, Vancouver
Collaborators (1)
North York General Hospital
OTHER
Royal Victoria Hospital Of Barrie
UNKNOWN
London Health Sciences Centre
OTHER
University of Alberta
OTHER
University of British Columbia
OTHER