NCT02341430

A Longitudinal Prospective Outcomes Study of Laparoscopic Abdominal Wall Hernia Repair Using Symbotex™ Composite Mesh

• Status: Completed
• Phase: Phase 4
• Study type: Interventional
• Enrollment: 50 (estimated)
• Sponsor: Anne Arundel Health System Research Institute · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This study is being done to test the efficacy of Symbotex™ as an effective synthetic mesh option in the repair of grade I and II ventral hernias.

Detailed description

This study is being done to validate the efficacy of Symbotex™ as an effective synthetic mesh option in the repair of grade I and II ventral hernias. It will also set the groundwork for a future clinical trial in which the efficacy of Symbotex® can be compared to other synthetic mesh products on the market.

Conditions

• Grade I Ventral Hernia
• Grade II Ventral Hernia

Interventions

Type	Name	Description
DEVICE	Symbotex™ Composite Mesh	Repair of a Grade I or II ventral hernia according to VHWG classification system with Symbotex™ Composite Mesh

Timeline

• Start date: 2016-01-01
• Primary completion: 2017-09-11
• Completion: 2018-12-31
• First posted: 2015-01-19
• Last updated: 2019-02-07

Locations

1 site across 1 country: United States