A Randomised Controlled Trial to compare between laparoscopic and Robotic Transabdominal preperitoneal inguinal hernia repair
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/07/043873
- Lead Sponsor
- AIIMS Jodhpur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All consenting adult patients (18years) with uncomplicated inguinal hernia coming to General Surgery OPD, AIIMS Jodhpur
Exclusion Criteria
1) Not consenting to participate in the study
2) Patients who need an open inguinal hernia repair.
3) Patient not fit to be operated under general anaesthesia
4) Not consenting to participate in the study
5) Patients who need an open inguinal hernia repair.
6) Patient not fit to be operated under general anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary objective: <br/ ><br>â??To compare the post-operative pain between two groups at 3 hours, 6 hours and at 12 hours <br/ ><br> <br/ ><br>Timepoint: 3 hours, 6 hours , 12 hours after surgery <br/ ><br>
- Secondary Outcome Measures
Name Time Method To compare the: <br/ ><br>â??Operative duration <br/ ><br>â??Rate of conversion to open <br/ ><br>â??Post-operative length of hospital stay <br/ ><br>â??Incidence of post-operative urinary retention <br/ ><br>â??Time (in days) to resume normal activities <br/ ><br>â??30 days complications <br/ ><br>Timepoint: 30 days