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3 Fixation Devices in Laparoscopic Ventral Herniotomy — FS  

Ventral Hernia Clinical Trial

Official title:
A Controlled Randomized Study of Protack, Securestrap and Glubran Glue as Fixation Devices in Laparoscopic Ventral Herniotomy

Clinical Trial Summary

Clinical, controlled, randomized, prospective study. Ventral hernias between 2(1.5)cm and 7 cm, laparoscopic surgery with intraperitoneal onlay mesh.

Three randomization groups of 25 patients giving a total of 75 patients. Mesh is fixated with either Protack, Securestrap or Glubran II. Primary outcome: postoperative pain on the 2nd postoperative day. Secondary outcomes: pain, quality of life, recurrence and adhesions at 1, 6, 12, 24, 36, 48 and 60 months postoperative.

Clinical Trial Description

see brief summary ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01534780
Study type Interventional
Source Horsens Hospital
Contact
Status Completed
Phase N/A
Start date April 2013
Completion date August 2017
View Details
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