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Mesh Fixation With a Synthetic Glue in Primary Inguinal Hernia Repair

Inguinal Hernia Clinical Trial

Official title:
Mesh Fixation With a Synthetic Glue in Primary Inguinal Hernia Repair

Clinical Trial Summary

Prospective observational study with mesh fixation using FDA approved synthetic glue,glubran 2 and standard mesh fixation with stiches in primary inguinal hernia repair surgery. The investigators aim is to recruit 150 patients for the study.

The outcomes The investigators would like to determine are : postoperative pain,recurrences and complication rates such as seromas.

Clinical Trial Description

Prospective observational study with mesh fixation using FDA approved synthetic glue,glubran 2 and standard mesh fixation with stiches in primary inguinal hernia repair surgery. The investigators aim is to recruit 150 patients for the study.

The outcomes The investigators would like to determine are : postoperative pain,recurrences and complication rates such as seromas. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02507830
Study type Observational
Source Rambam Health Care Campus
Contact Adel Abu_Salih, MD
Phone 972-4-8541308
Email a_abu_salih@rambam.health.gov.il
Status Recruiting
Phase N/A
Start date August 2015
Completion date July 2017
View Details
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