About this trial
The objective of this study is to establish the extent to which mesh improves quality of life and surgical outcomes following hernia repair.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
abdominal hernia repair using mesh
Disqualifiers
less than 18 years old
Trial population
Multihospital system inclusive of all abdominal hernia repairs using mesh
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Hernia recurrence rate
Should the hernia repair fail and the hernia reappears, this is counted as a recurrent hernia.
Patient quality of life
Quality of life before and after surgery will be compared using various self-reported assessment tools/questionnaires.
Secondary outcomes
Postoperative infection rate
Infection related to hernia repair or mesh use will be reported.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Endeavor Health
Lead sponsor
Medtronic
Collaborator