Chronic Pain Clinical Trial
Official title:
A Randomised Controlled Trial Comparing Total Extra-Peritoneal (TEP) to Lichtenstein Inguinal Hernia Repair Concerning Physical Sequelae and Quality of Life at One and Three Years - the TEPLICH Trial
The purpose of this study is to se if there is a difference regarding chronic pain and sexual
dysfunction one and tree years after laparoscopic un fixated preperitoneal mesh versus gold
standard open fixated on lay mesh in inguinal hernia surgery.
Long term cross-sectional follow-up comparing different instruments for measurement of
chronic pain.
Prospective randomized study comparing total extraperitoneal patch TEP versus open onlay mesh
according to Lichtenstein in primary unilateral inguinal hernias in men between 30 to 75
years of age. Non fixated polypropylene mesh is used in the TEP operation and fixated light
weight polypropylene mesh is used in the Lichtenstein procedure. The aim is to study
chronical pain and sexual dysfunction. Clinical examination according nerve function, hernia
status and genital findings are performed together with a questionnaire including SF36,
Inguinal Pain Questionnaire(IPQ), sexual function are registered preoperatively, one and tree
years postoperatively.
Cross-sectional follow-up in median 7.5 years using enquiries for comparison of different
pain instruments to evaluate the effect of chronic pain on physical activity.
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