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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

Analgesic Efficacy of Erector Spinae Block versus Quadratus Lumborum III Block in patients undergoing Unilateral Percutaneous Nephrolithotomy Surgery under General Anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/053543
Enrollment
78
Registered
2023-06-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N202- Calculus of kidney with calculus of ureter

Interventions

Intervention1: Dr.Pooja Singh: Associate professor, Department of Anaesthesiology, AlIMS Bhopal, 462024,Madhya pradesh India Control Intervention1: Dr.Yamini Arora: Post graduate Resident, Department

Sponsors

Dr Pooja Singh
Lead Sponsor

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
1.To determine & compare the time of the first analgesic. 2.To determine and compare the total perioperative opioid consumption in 24 hours 3.To determine and compare the rate of complications, time of ambulation and length of hospital stay. (.between the group E and Q)Timepoint: From arrival in postoperative recovery room upto discharge from hospital .

Countries

India

Contacts

Public ContactDr Pooja Singh

All India Institute of Medical Sciences

YAMINIA.jr2022@aiimsbhopal.edu.in9463458927

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026