Comparison treatment outcomes use of two classic and preperitoneal surgery methods in inguinal hernia repair
Not Applicable
- Conditions
- inguinal herniorrhphy.Hernia with both gangrene and obstruction is classified to hernia with gangrene
- Registration Number
- IRCT2016030826974N1
- Lead Sponsor
- Vice Chancellor for research of Lorestan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 150
Inclusion Criteria
having inguinal hernia, candidate for classic herniorrhaphy, candidate for preperitoneal herniorrhaphy, satisfaction to enter to study.
Exclusion criteria: diabetes, bleeding disorders, aspirin and corticosteroid consumption.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before intervention and two months after intervention. Method of measurement: questionnaire.;Duration of operation. Timepoint: after intervention. Method of measurement: Clock-Patient case.
- Secondary Outcome Measures
Name Time Method Recurrence. Timepoint: 3, 4, 5, 6 and 12 months after intervention. Method of measurement: questionnaire.;Hematoma. Timepoint: 3, 4, 5 and 6 months after intervention. Method of measurement: questionnaire.;Seroma. Timepoint: 3, 4, 5 and 6 months after intervention. Method of measurement: questionnaire.;Patient satisfaction rate. Timepoint: 6 months after intervention. Method of measurement: questionnaire.