Lighter mesh may mean less pain after hernia repair
NCT ID NCT00451893
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compared two types of surgical mesh used to repair inguinal hernias in 412 men. One mesh was heavy-weight (90 g/m²) and the other was light-weight (28 g/m²). The goal was to see if the lighter mesh caused less pain and improved quality of life after surgery. Patients were randomly assigned to surgeons trained in one of the two mesh types.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- surgical mesh (light-weight or heavy-weight polypropylene)
- What this could lead to
- If the light-weight mesh works better, it could mean less long-term pain and better quality of life for hernia patients.
- What could go wrong
- This is a completed trial, so results are already known. The difference between meshes may be small, and individual results can vary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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412 people
The number who actually took part.
- Started
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Sep 2006
- Finished
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Apr 2019
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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25 years and older
- Sex
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Male participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male, age 25 years or older * Reducible, unilateral, inguinal hernia (not femoral hernia) that has not been operated on before Exclusion Criteria: * The patient is not able or do not want to give written informed consent * The patient is not suitable for an operation in local anesthesia * Anticoagulant medication or a known coagulation disorder
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Department of Surgical and Perioperativ Sciences, Umeå University Hospital
Umeå, SE 90185, Sweden
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Östersund Hospital
Östersund, SE 83183, Sweden
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