Comparison of pain relieving efficacy in transverse abdominal plane block and erector spinae plane block in a patient posted following pcnl under general anaesthesia
Phase 1
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/064116
- Lead Sponsor
- Mahatma Gandhi Medical College And Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients scheduled for PCNL surgery.
Patients of either sex having age 18-65years.
Patients who are willing to participate in this study by written and informed consent.
Patient fulfilling criteria of American Society of Anesthesiology (ASA) of Classes I/ II.
Exclusion Criteria
Patients with ASA physical status grade III/IV
Patients with history of drug allergy
Infection at local site
H/o drug abuse, psychiatric disorder, chronic pain
coagulation abnormalities
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the analgesic effect of subcostal transversus abdominal plane block and erector spine block will be assessed at the end of operation by haemodynamic variability and postoperatively by visual analog scale(VAS), if VAS is more than 4 the patient will receive a rescue dose of 1mg/kg/dose of tramadol.Timepoint: VAS scores will be assessed at intervals of 30 min, 60 min, 2nd hour, 4th hour and then followed fourhourly(8, 12, 16, 20, 24) up to 24 hour postoperatively.
- Secondary Outcome Measures
Name Time Method mean blood pressure, heart rate, patient satisfactionTimepoint: The effects will be assessed for 24 hrs post procedure