An Observational Study of Recurrence of Inguinal Hernia After Repair Using Parietex Lap-Progrip
Not Applicable
Recruiting
- Conditions
- inguinal herunia
- Registration Number
- JPRN-UMIN000020097
- Lead Sponsor
- Juntendo University Urayasu HospitalSurgical Department
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
1)Recurrent inguinal hernia 2)Emergency surgery 3)Patients with incarcerated hernia 4)Other patients judged by the investigator to be inappropriate to participate in this study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hernia recurrence rate within 2 year following the procedure
- Secondary Outcome Measures
Name Time Method 1)Postoperative pain (Numeric Rating Scale) 2)Adverse events (bleeding, selome, hematoma, infection, edema, allergic reaction to the products structural materials, intestinal obstruction, and urinary retention due to anesthesia) 3)Patient satisfaction level 4)Operative time 5)Length of hospital stay 6)No of Parietex Lap-Progrip used, cost 7)Whether trimming is required or not