To compare the side effects and efficacy of the two surgical instruments used for laparoscopic hernia surgery in patients with hernia-A Randomised Control Trial
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/03/040855
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
all elective patients above 18 yrs of age who are undergoing elective laparoscopic inguinal repair
Exclusion Criteria
bilateral inguinal hernia
emergent inguinal hernia repairs
recurrent inguinal hernia with prior preperitoneal mesh
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the post operative pain score at 6 th hour postoperatively between two surgical techniquesTimepoint: 2 years
- Secondary Outcome Measures
Name Time Method to assess the impact of telescopic dissection or balloon dissection on operative time, intraoperative complications and surgical site occurence for creation of extraperitoneal space during laparascopic TEP inguinal hernia repairTimepoint: 2 years