Comparison treatment outcomes use of two types of mesh in inguinal hernia repair
Not Applicable
- Conditions
- Inguinal hernia.Inguinal hernia
- Registration Number
- IRCT2014050811560N8
- Lead Sponsor
- Deputy of Research,Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
age between 18-80 years old; non emergent unilateral primary inguinal hernia.
Exclusion criteria: drug abusers; pregnancy; history of Diabetes mellitus; history of uncontrolled hypertension; history of psychological disorders and use of psychoactive drugs.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 1-3-6-12 months after surgery. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Hernia recurrence. Timepoint: 1-3-6-12 months after surgery. Method of measurement: Physical Examination.
Related Research Topics
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What are the molecular mechanisms of conventional and sutureless mesh in inguinal hernia repair?
How does the sutureless mesh compare to standard-of-care treatments in primary inguinal hernia outcomes?
Are there specific biomarkers that predict better outcomes with sutureless mesh in inguinal hernia repair?
What are the potential adverse events associated with conventional and sutureless mesh in hernia surgery?
What are the current trends in mesh technology for inguinal hernia repair beyond conventional and sutureless types?