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Clinical Trial Summary

Patients with a primary unilateral inguinal hernia are randomized to Lichtenstein's operation or Prolene Hernia System to repair their groin hernia. Follow up for three years with a total number of 4 clinical examinations. End point is postoperative pain and recurrences.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00184483
Study type Interventional
Source Norwegian University of Science and Technology
Contact
Status Completed
Phase N/A
Start date October 2001
Completion date December 2015

See also
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