Randomised controled trial comparing the effect of a new self-gripping semi-resorbable Parietene Progrip mesh and the sutured Polypropylene mesh on the incidence of chronic inguinodynia in Lichtenstein hernioplasty.
Completed
- Conditions
- groin herniahernia inguinalis10040795
- Registration Number
- NL-OMON33251
- Lead Sponsor
- Groene Hart Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 400
Inclusion Criteria
1. Capacitated male person, age 18 years or older
2. Unilateral inguinal hernia
Exclusion Criteria
1. Concurrent femoral hernia
2. Incarcerated inguinal hernia
3. ASA 4 or more
4. Adequate follow up impossible because of mental retardation, dementia, foreign language speaker.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>1. Amount of post-operative and chronic nociceptive and neuropathic groin pain.<br /><br>2. Recurrence rate</p><br>
- Secondary Outcome Measures
Name Time Method <p>1. Peroperative and post-operative complications like infection, formation of<br /><br>haematoma or seroma.<br /><br>2. Operating time<br /><br>3. Costs<br /><br>4. Easiness of use<br /><br>5. Return to work and daily activities<br /><br>6. quality of life</p><br>