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To assess pain reducing efficacy of Ultrasound guided Erector Spinae Block versus Quadratus Lumborum III Block in patients undergoing Unilateral Percutaneous Nephrolithotomy Surgery under General Anesthesia

Not Applicable
Conditions
Health Condition 1: N202- Calculus of kidney with calculus of ureter
Registration Number
CTRI/2023/06/053543
Lead Sponsor
Dr Pooja Singh
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Study will include patients between 18 to 65years of either sex with ASA physical status 1 to 3 planned for elective percutaneous nephrolithotomy

Exclusion Criteria

Patientâ??s refusal to the procedure.

Contraindications to regional technique e.g., allergy to local anesthetic drugs, infection around site of block, any coagulation disorder, sepsis

Body mass index > 35kg/m2

Pregnancy

Physical or mental disorders that would interfere with evaluation of pain.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine and compare postoperative pain relief using the numeric rating scale (NRS) score between the group E and group QTimepoint: At 1 hour, 2 hours, 6 hours, 12 hours and 24 hours postoperatively at rest and during activity
Secondary Outcome Measures
NameTimeMethod
1.To determine & compare the time of the first analgesic. <br/ ><br>2.To determine and compare the total perioperative opioid consumption in 24 hours <br/ ><br>3.To determine and compare the rate of complications, time of ambulation and length of hospital stay. <br/ ><br>(.between the group E and Q)Timepoint: From arrival in postoperative recovery room upto discharge from hospital .
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