Study protocol for a randomised clinical trial comparing TREPP versus Lichtenstein*s technique in Inguinal hernia patients
Withdrawn
- Conditions
- Inguinal hernia10040795
- Registration Number
- NL-OMON45767
- Lead Sponsor
- Medisch Centrum Leeuwarden
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 750
Inclusion Criteria
Adults with a clinically apparent primary unilateral inguinal hernia
Age > 18 years
ASA classification 1-3
Signed informed consent
Exclusion Criteria
Recurrent inguinal hernia
bilateral inguinal hernia
ASA class 4
Acute incarcerated inguinal hernia
psychiatric disease or other reasons making follow-up or questionnaires unreliable
previous preperitoneal surgery (e.g. radical prostatectomy)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Chronic postoperative inguinal pain</p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcomes are complications, recurrences, sexual complaints, bleeding,<br /><br>time of return to daily activities and operating time. </p><br>