Clinical evaluation of postoperative quality-of-life in the open mesh repair for inguinal hernia
Not Applicable
- Conditions
- Inguinal hernia
- Registration Number
- JPRN-UMIN000000946
- Lead Sponsor
- Showa university fujigaoka hospital Surgery, 1-30, fujigaoka, aoba-ku, yokohama-city, kanagawa, Japan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
Not provided
Exclusion Criteria
1. Pregnant 2. The case with pneumonitis, peritonitis, ileus, perforation, intraperitoneally infection or urinary infection. 3. The case with Bleed, clotting disorder, wound healing disorder. 4. The case with mental illness such as depression and dementia. 5. Relapsing hernia 6. Incarcerated hernia which cannot be reduced. 7. The case with peripheral nerve disorder.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison study of quality-of-life in the patients 1, 3, 6 and 12 month after the operation using SF-36.
- Secondary Outcome Measures
Name Time Method Comparison study of postoperative pain (1, 2, 3, 7 day and 1, 3, 6, 12 month after the operation), complication and recurrence.