A trial to compare pain control after PCNL surgery between Erector Spinae muscle plane block and renal injection through the nephrostomy tube with 0.25% injection Levobupivacaine administered randomly.
Phase 2
Completed
- Conditions
- Health Condition 1: - Health Condition 2: N200- Calculus of kidney
- Registration Number
- CTRI/2022/11/047001
- Lead Sponsor
- Government of West Bengal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 78
Inclusion Criteria
Patients with age between 18 to 65 years and of American Society of Anesthesiologist (ASA) category 1 or 2 of both sexes, who give informed consent to participate in the study and who undergo PCNL surgery in our institute during the study period.patient having single access PCNL.
Exclusion Criteria
) Significant residual stones ( >1 cm in diameter) after surgery and the need for a second look
(b) Bleeding diathesis
(c) A solitary kidney;
(f) Routine antidepressant, corticosteroid, pain medication, or anticonvulsant usage,
(g) A mental state preventing the effective use of VAS score.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome-Time to first rescue analgesia (hrs) ie, time from successful completion of block till first administration of rescue analgesic.Timepoint: Primary outcome-Time to first rescue analgesia (hrs) ie, time from successful completion of block till first administration of rescue analgesic.
- Secondary Outcome Measures
Name Time Method VAS score at time intervals, total rescue analgesic required, SBP,DBP, heart rate at intervals, adverse effectsTimepoint: Assessment at intervals 1 ,2,4,6,12,18 and 24 hours postoperatively.