INguinal hernia: operative or Conservative Approach (INCA TRIAL)?
Recruiting
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 800
Inclusion Criteria
1. Unilateral inguinal hernia;
2. Males;
Exclusion Criteria
1. Gender: female;
2. Bilateral inguinal hernia;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The mean of 4 pain/discomfort scores during a follow-up period of 3 years.
- Secondary Outcome Measures
Name Time Method The Quality Adjusted Life Years (QALY) with quality weights measured with the EuroQol and in a sensitivity analysis with a transformed SF-36 utility weight, medical and non-medical costs and the event-free survival at 3 years.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms underlying inguinal hernia recurrence after conservative management in the INCA TRIAL?
How does the INCA TRIAL compare the effectiveness of laparoscopic versus open hernia repair in reducing postoperative complications?
What biomarkers are used in the INCA TRIAL to predict patient response to conservative treatment versus surgical intervention?
What are the potential adverse events associated with elective hernia repair in the INCA TRIAL and how are they managed?
How does the INCA TRIAL evaluate the long-term outcomes of conservative approaches versus surgical repair in hernia subtypes?