NCT00184483
Completed
Not Applicable
Randomized Multi Site Trial Comparing Lichtensteins Operation and Prolene Hernia System in Inguinal HErnia Repair.
ConditionsInguinal Hernia
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Inguinal Hernia
- Sponsor
- Norwegian University of Science and Technology
- Enrollment
- 405
- Locations
- 1
- Primary Endpoint
- pain postoperative
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief 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.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Primary unilateral groin hernia in adult
Exclusion Criteria
- •recurrence warfarin treatment bilateral groin hernia
Outcomes
Primary Outcomes
pain postoperative
Time Frame: 3 years
Secondary Outcomes
- Recurrences after groin hernia repair(3 years)
Study Sites (1)
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