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Clinical Trial Summary

In this study the researchers want to compare fibrin glue versus tacked fixation in fixation of the mesh in laparoscopic groin hernia repair. The primary endpoints are early pain in the first 3 days postoperative days. Moreover, the researchers investigate general well-being, fatigue, seroma, haematoma, postoperative nausea and vomiting. Thirdly, they are investigating chronic pain and clinical recurrence.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01000116
Study type Interventional
Source University Hospital Koge
Contact
Status Completed
Phase N/A
Start date September 2009
Completion date February 2012

See also
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Completed NCT02240550 - A Comparative Clinical Study to Evaluate the Effectiveness of ProFlor vs. Lichtenstein for Inguinal Hernia Repair N/A
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Active, not recruiting NCT04328597 - Portuguese Inguinal Hernia Cohort (PINE) Study
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Completed NCT03590145 - Reliability of the Doha Agreement Classification of Groin Pain