At a glance
ClinicalIndex Comparison RecordN/AUnknown· 267 enrolled
Drug / intervention
Mesh implementationdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Intraperitoneal Mesh-Implementation After Laparotomy to Reduce Risk of Incisional Hernia: a Prospective Randomized Controlled Trial
In Brief
A clinical study evaluating Mesh implementation for Incisional Hernia. Targeting 267 participants across 1 site.
Detailed Summary
Aim of the study is to evaluate the risk reduction of intraperitoneal mesh-implementation after laparotomy (Group 1) in a randomized control trial compared with patients with standard abdominal closure (Everett-suture). This is the primary endpoint. Second endpoints are the feasibility of mesh-implementation even after colorectal surgery, find risk factors for wound infection and incisional hernia.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsIncisional Hernia
CountriesSwitzerland
Collaborators--
Timeline
N/AUnknownOverdue
20082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartMar 2008
First PostedOct 2009
Primary CompletionMay 2013
Study CompletionJun 2020
TodayJul 2026
First PostedOct 28, 2009
Enrollment StartMar 1, 2008
Primary CompletionMay 1, 2013
Study CompletionJun 1, 2020
TodayJul 2, 2026
Enrollment to primary: 5.2 yearsPosted 16.7 years ago
Interventions
Mesh implementationdevice
Prophylactic intraperitoneal mesh implantation in laparoscopic surgery to prevent incisional hernia.