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Comparison of Self-adhering Mesh and Conventional Mesh in Inguinal Hernia Repair.

Not Applicable
Terminated
Conditions
Inguinal Hernia
Interventions
Procedure: Open anterior inguinal hernia repair
Registration Number
NCT01334775
Lead Sponsor
Maastricht University Medical Center
Brief Summary

Inguinal hernia repair coincides with a high rate of postoperative pain, extending to over a year in 10-20% of patients. Although this is of major concern, early postoperative pain also has an important impact on patients and their ability to regain normal work and activities. Since inguinal hernia repair is the most frequently performed operation worldwide, a small reduction in loss of workdays can already have significant impact on financial issues. As for the origin of the pain, it might be the result of local inflammation caused by the mesh material, but also by nerve entrapment due to fixation techniques. The development of a new mesh which enables sutureless fixation, Cousin Biotech® Adhesix™, may overcome pain related to fixation techniques used in the open hernia repair procedure according to Lichtenstein. Furthermore, the Cousin Biotech® Adhesix™ mesh has already been in use in our institutions and surgeons familiarized themselves with the application.

The investigators would like to conduct a multicentre randomised controlled clinical trial to compare the difference in early postoperative pain after unilateral primary inguinal hernia repair in males. The procedures will be performed in day surgery. Early postoperative pain is defined as the pain during the first month, with a special interest in the first two weeks. In addition, the investigators want to measure the possible benefit in terms of time to return to work, daily activities, quality of life, operation length, complications and long term postoperative pain.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
Male
Target Recruitment
70
Inclusion Criteria
  • Male
  • Primary, unilateral inguinal hernia
  • Age ≥18 years
  • Social status: professionally employed
  • ASA-score I-III
  • Signed informed consent
  • Elective surgery
Exclusion Criteria
  • Female
  • Bilateral and/or recurrent inguinal hernia
  • Femoral or scrotal hernia
  • Vasectomy
  • Social status: unemployed
  • Chronic use of pain medication
  • Symptomatic acute hernia (i.e. bowel obstruction, incarceration, strangulation, peritonitis or perforation of bowel contents)
  • ASA-score IV or above
  • Incapacitated adult or no signed informed consent
  • Patient is unable to speak Dutch

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental - Cousin Biotech AdhesixOpen anterior inguinal hernia repairPlacement of a self-adhering (sutureless) surgical mesh in open anterior inguinal hernia repair
Conventional - Cousin Biotech Biomesh P8Open anterior inguinal hernia repairPlacement of the conventional (sutured) surgical mesh in open anterior inguinal hernia repair
Primary Outcome Measures
NameTimeMethod
Difference in early postoperative pain scores0-4 weeks after surgery

Measured with VAS-scores

Secondary Outcome Measures
NameTimeMethod
Number of days to return to work0-12 months after surgery
Number of patients with complications/adverse events0-12 months after surgery

All adverse events/complications are recorded (i.e. infection, recurrence, bleeding)

Number of days to return to normal daily activities0-12 months after surgery
Difference in long-term postoperative pain scores4 weeks - 12 months after surgery

Measured with VAS-scores

Differences in reported Quality of life0-12 months after surgery

Measured with SF-36 questionnaire

Differences in use of analgesics0-12 months after surgery

Measured: frequency, dose and type.

Trial Locations

Locations (4)

VieCuri Medical Centre, dept. of General Surgery

🇳🇱

Venlo, Netherlands

Academic Medical Centre Amsterdam, dept. of Surgery

🇳🇱

Amsterdam, Netherlands

Maastricht University Medical Centre, dept. of General Surgery

🇳🇱

Maastricht, Netherlands

Orbis Medical Centre

🇳🇱

Sittard-Geleen, Netherlands

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