Comparison of two methods of groin hernia repair surgery
Not Applicable
- Conditions
- Condition 1: Inguinal Hernia. Condition 2: Inguinal Hernia.Bilateral inguinal hernia, without obstruction or gangreneUnilateral or unspecified inguinal hernia, without obstruction or gangrene
- Registration Number
- IRCT201202038911N1
- Lead Sponsor
- Ahvaz Jundishapour University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
all men and women between 25-90 y. who have Inguinal Hernias. Exclusion criteria: recurrent inguinal hernia; concomitant femoral hernia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incision length. Timepoint: At the end of operation. Method of measurement: in cm, with a sterile ruler.;Operation duration. Timepoint: From incision of skin till the last suture, intraoperative. Method of measurement: in minute, with a standard watch.
- Secondary Outcome Measures
Name Time Method Surgery site Hematoma. Timepoint: During first 48 hours. Method of measurement: Blood accumulation under surgery site, By needle aspiration.;Surgery site Seroma. Timepoint: During first 48 hours. Method of measurement: Interstisial fluid accumulation, By needle aspiration.;Urinary retention. Timepoint: During first 24 hours. Method of measurement: Deep sensation and bulging of lower abdomen, By sundage.;Surgery site infection. Timepoint: During first 48 hours AND within first week. Method of measurement: Tenderness, erythema, buldging, pus discharge, By surgeon experience and exam.;Anesthesia of inguinal region. Timepoint: During first week and 2 month later. Method of measurement: Murmur and deepness of region, By history and exam.;Hernia recurency. Timepoint: 2 month after surgery. Method of measurement: Deep sensation and bulging of region after activity. By Ultrasonography and exam.