Clinical Trials Logo

Clinical Trial Summary

Chronic pain rate is from 0 to 50% after prosthetic groin hernia repair. We compared two anterior technique positioning the mesh in the pre-trasversalis space vs preperitoneal space to assess any differences in term of chronic pain and early and late complications


Clinical Trial Description

Chronic pain is evaluated in all presenting types (achy, dull, etc.) moreover foreing body sensation, wall stiffness, paresthesia and numbness are controlled in each patients. Limiting of daily, working, sport and sexual activities (disejaculation) are reported as well. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01350830
Study type Interventional
Source San Bonifacio Hospital
Contact
Status Completed
Phase Phase 4
Start date November 2007
Completion date January 2011

See also
  Status Clinical Trial Phase
Completed NCT01211067 - Study of Histological Findings of the Internal Inguinal Ring in Patients With Indirect Inguinal Hernia N/A
Active, not recruiting NCT04634032 - Gene Expression and DNA Variation Analysis of Sacs to Identify the Pathophysiology of Indirect Inguinal Hernia