Clinical Trials Directory

Trials / Terminated

TerminatedNCT01201564

Comparative Study Matching Intraperitoneal Onlay Mesh (IPOM) and Sublay Mesh to Treat Umbilical Hernia

Prospective Randomized Multicenter Trial Comparing Laparoscopic (IPOM) vs. Sublay Mesh Plasty for Umbilical Hernia in Adults

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
306 (actual)
Sponsor
University Hospital, Basel, Switzerland · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is designed to compare two techniques for operative care of umbilical hernia in adults regarding wound complications, wound side fluid collections, recurrence rate, postoperative pain, duration of hospitalization and quality of life. The IPOM technique provides mesh positioning directly into the abdominal cavity onto the defect under laparoscopic control while in sublay position the mesh is placed directly behind the rectus muscle after small incision close to the belly button.

Conditions

Interventions

TypeNameDescription
PROCEDUREintraperitoneal onlay mesh repairThe IPOM technique provides mesh positioning directly into the abdominal cavity onto the defect under laparoscopic control while in sublay position the mesh is placed directly behind des rectus muscle after small incision close to the belly button.
PROCEDUREsublay mesh repairThe IPOM technique provides mesh positioning directly into the abdominal cavity onto the defect under laparoscopic control while in sublay position the mesh is placed directly behind des rectus muscle after small incision close to the belly button.

Timeline

Start date
2010-07-01
Primary completion
2018-12-01
Completion
2018-12-01
First posted
2010-09-14
Last updated
2019-05-07

Locations

3 sites across 2 countries: Germany, Switzerland

Source: ClinicalTrials.gov record NCT01201564. Inclusion in this directory is not an endorsement.