comparison of post operative outcomes after two methods of mesh fixation in laparoscopic inguinal hernia repair
Not Applicable
- Conditions
- nilateral Inguinal hernia.Unilateral or unspecified inguinal hernia, without obstruction or gangrene
- Registration Number
- IRCT201202118972N1
- Lead Sponsor
- Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
age 18-70; good general condition for general anesthesia; good condition for TAPP procedure
Exclusion criteria:
Laparascopic surgery contraindications such as cardiovascular problems and portal hypertension; ASA IV or V; drug abuse; general surgery contraindications; laparascopic pelvic surgery contraindications; huge scrotal hernia; bowel obstruction; bowel incarceration; bowel perforation; peritonitis; local or systemic infection; previous hernia repair with mesh; history of prostatectomy; life expectancy less than 2 years; diabetic poly neuropathy; spondyloarthrosis with dorsal lumbar nerves involvement
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anti pain medication requirement after surgery. Timepoint: daily for 1 week after surgery. Method of measurement: Questionnaire.;Pain severity after surgery. Timepoint: daily for 1 week after surgery. Method of measurement: VAS Questionnaire.;Seroma formation. Timepoint: 1 week, 1, 3 & 6 months after surgery. Method of measurement: Questionnaire.
- Secondary Outcome Measures
Name Time Method Days of hospital stay. Timepoint: Daily. Method of measurement: Questionnaire.;Reccurence. Timepoint: 1 week, 1,3 & 6 months after surgery. Method of measurement: Physical exam.;Days befor return to work after surgery. Timepoint: Daily. Method of measurement: Questionnaire.;Surgery duration. Timepoint: Minutes. Method of measurement: Questionnaire.