A Multi-site Trial Comparing Lichtensteins Operation and Prolene Hernia System in Inguinal HErnia Repair
NCT ID: NCT00184483
Last Updated: 2020-09-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
405 participants
INTERVENTIONAL
2001-10-31
2015-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Lichtenstein's operation
Patients with a primary unilateral inguinal hernia are randomized to Lichtenstein's operation to repair their groin hernia
Lichtenstein's operation
Lichtenstein's operation to repair primary unilateral inguinal hernia
Prolene Hernia System
Patients with a primary unilateral inguinal hernia are randomized to Prolene Hernia System to repair their groin hernia
Prolene Hernia System
Prolene Hernia System to repair primary unilateral inguinal hernia
Interventions
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Lichtenstein's operation
Lichtenstein's operation to repair primary unilateral inguinal hernia
Prolene Hernia System
Prolene Hernia System to repair primary unilateral inguinal hernia
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
20 Years
80 Years
ALL
No
Sponsors
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Sorlandet Hospital HF
OTHER_GOV
Voss Sykehus
UNKNOWN
Haraldsplass Deaconess Hospital
OTHER
Sykehuset Ostfold
OTHER
Norwegian University of Science and Technology
OTHER
Responsible Party
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Principal Investigators
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Helge E Myrvold, MD PhD
Role: STUDY_DIRECTOR
Norwegian University of Science and Technology
Locations
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St Olavs Hospital
Trondheim, , Norway
Countries
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Other Identifiers
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Norwegian Hernia Study
Identifier Type: -
Identifier Source: org_study_id
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