PROphylactic Mesh to Prevent Incisional Hernias at the Former Stoma Site:
the PROMISS-trial (PROMISS)
Approximately 7000 stomata are created in the Netherlands every year. The occurrence of a parastomal herniation is high, with a reported incidence of 4-48%. Also, the former stoma site is at increased risk for the development of an incisional hernia. A clinical incisional hernia rate of 30% is reported after stoma reversal. Herniation can cause pain, deformity and possibly incarceration, which results in a significant impact on the quality of life of the patient.
The hypothesis of this study is that the use of a prophylactic mesh at the time of stoma formation leads to a lower incidence of incisional hernias after stoma reversal, an improved quality of life and therefore a possible cost reduction in healthcare.
To evaluate the incidence of incisional hernias after stoma reversal after preventive mesh placement compared to no mesh placement. In addition, we aim to assess the effect of preventive mesh placement on the quality of life and the effect on healthcare cost reduction by avoiding re-intervention.
A multicentre double blind randomized controlled trial with a total follow up of 24 months.
Adults (18-99) undergoing bowel resection with the formation of a temporary stoma.
A preventive mesh will be placed using a sublay keyhole technique (pre-peritoneal, retromuscular) at stoma formation. The mesh will be left in situ after stoma reversal and the hole in the mesh will be closed, to prevent incisional herniation.
Main study parameters/endpoints:
Primary: Incidence of incisional hernias after stoma reversal
Secondary: Quality of life, stoma related prolapse or parastomal herniation, cost effectiveness and mesh related complications.
Nature and extent of the burden and the risks associated with participation, benefit and group relatedness:
The standard surgical procedure for the treatment of parastomal hernias is used in a prophylactic fashion. As this is standard care in parastomal hernias the risks are minimal. The mesh that is used is CE approved. The burden of participation in this study is minimal for the patient all follow-up visits coincide with the regular visits for colorectal cancer. Hence, no extra outpatient department visits, and even no additional diagnostics nor other medical procedures that could potentially burden the patient, are required.
Contact: Nicole D Bouvy, MD, PhD +3143-3875492 firstname.lastname@example.org
Contact: Sebastiaan Steensel, MD +3143-3872354 email@example.com
Link to the publication at the U.S. National Library of Medicine, Clinical Trials