A Randomoised,Prospective, Double Blinded Study To Compare The Efficacy Of Ultrasound Guided Transversus Abdominis Plane Block and Erector Spinae Plane Block in Minimally Invasive Nephrectomy Surgeries
Overview
- Phase
- Phase 2/3
- Status
- Not yet recruiting
- Sponsor
- SRM Institutes For Medical Sciences
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- 1)To observe intraoperative Remifentanil requirement and the pain score using Visual Analog Scale (VAS) score for first 24 hours,postoperative Tramadol requirement for first 24 hours
Overview
Brief Summary
This study is a randomised ,prospective,double blinded comparing the efficacy of ultrasound guided Transversus Abdominis Plane Block and Erector Spinae Plane Block in Minimally Invasive Nephrectomy Surgeries.Primary outcomes will be intraoperative Remifentanil requiremet,the pain score using Visual Analog Scale (VAS) score for first 24 hours,the postoperative Tramadol requirement for first 24 hours.secondary outcomes will be the incidence of hemodynamic disturbances during perioperative period,the incidence of side effects of opioids such as postoperative nausea, vomiting, sedation and respiratory depression.
Study Design
- Study Type
- Interventional
- Allocation
- Coin toss, Lottery, toss of dice, shuffling cards etc
- Masking
- Participant and Investigator Blinded
Eligibility Criteria
- Ages
- 20.00 Year(s) to 70.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •ASA grade 1 and 2,Any gender ,Age 20 to 70 years ,BMI 18 to 30 ,Patients willing to participate in the study ,Patients admitted for minimally invasive nephrectomy surgery ,No history of allergy to Local anaesthetics.
Exclusion Criteria
- •ASA grade 3, 4, 5,Pregnant and lactating mother,Age less than 20 years and more than 70 years,Obese individuals with BMI more than 30,Chronic history of Opioid abuse,History of allergy to Local anaesthetics,Patients not willing to participate in this study.
Outcomes
Primary Outcomes
1)To observe intraoperative Remifentanil requirement and the pain score using Visual Analog Scale (VAS) score for first 24 hours,postoperative Tramadol requirement for first 24 hours
Time Frame: 12 months
Secondary Outcomes
- 1) To observe the incidence of hemodynamic disturbances during perioperative period(2) To observe the incidence of side effects of opioids such as postoperative nausea, vomiting, sedation and respiratory depression)
Investigators
shanmugapriya g
SRM INSTITUTES FOR MEDICAL SCIENCES