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PHS, Lichtenstein Mesh, and PerFixPlug for Primary Inguinal Hernia Repair - 3 Years Results

Phase 4
Completed
Conditions
Hernia, Inguinal
Interventions
Procedure: Lichtenstein mesh
Procedure: PerFix Plug®
Procedure: Prolene® Hernia System
Registration Number
NCT00580177
Lead Sponsor
Göteborg University
Brief Summary

Three different techniques for the surgical repair of groin hernias are compared. Focus has been set on operation times, time to full return of functional abilities like walking in stairs etc, and if any technique has more complications than the others. Three years results are presented in the study.

Detailed Description

Dissection requirements differ between various methods for inguinal hernia repair, which may effect operation times, pain response and possibly recovery time. The objectives of this study were to establish if any differences concerning these aspects could be detected after three principally different techniques for primary inguinal hernia repair.

472 men between 30 and 75 years with primary inguinal hernias were included in a prospective controlled study and randomised to Lichtenstein mesh (L), PerFix Plug® (P) or the Prolene® Hernia System (PHS) procedure. All patients were seen and data were collected after 2 weeks, 3 months, 1 year, and 3 years.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
472
Inclusion Criteria
  • Age 30-75 years
  • Men
  • Primary inguinal hernia
  • ASA I-III
Exclusion Criteria
  • > 75 years
  • Females
  • ASA IV
  • Previous ipsi-lateral hernia surgery
  • Drug or alchol abuse
  • Severe illness

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
LLichtenstein meshThe Lichtenstein procedure for repair of inguinal hernia (Single On-lay patch)
PPerFix Plug®The well-konown PerFixPlug technique for inguinal hernia repair.
PHSProlene® Hernia SystemThe well-known Prolene Hernia System method for inguinal hernia repair.
Primary Outcome Measures
NameTimeMethod
Time until full functional recovery2 weeks, 3 months, 1 year, 3 years
Operation timeRegistered after completion of surgery
Pain after operation measured on a VAS-scale and amount of consumed analgesicsDay 1-14, 3 months, 1 year, 3 years after surgery
Secondary Outcome Measures
NameTimeMethod
Complication rate2 weeks, 3 months, 1 year, 3 years
Aptness for beeing performed under local anaesthesiaDuring surgery

Trial Locations

Locations (1)

Frolunda Specialist Hoospital/University of Gothenburg, Lundby Hospital, Molndals Hospital/Sahlgrens University Hospital

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Gothenburg, Vastra Gotalandsregionen, Sweden

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