Erector Spinae Block vs Conventional Analgesia for Postoperative Analgesia in PCNL

Not Applicable

Not yet recruiting

• Conditions: Percutaneous Nephrolithotomy (PCNL)
• Interventions: Procedure: Sonographic guided Erector spinae plane block; Drug: Intravenous opioid

• Registration Number: NCT06935006
• Lead Sponsor: Sohag University

Brief Summary

50 adult patients scheduled for percutaneous nephrolithotomy in Sohag university hospitals will be devided in two groups one of them will receive Sonographic guided erector spinae plane block using 20 ml volume of bupivacaine 0.25 percent and the other will receive conventional analgesia of 0.1 mg/kg IV morphine

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2025-03-09
• Status Verified: 2025-04
• Study First Submitted QC: 2025-04-11
• Last Update Submitted: 2025-04-11
• Study First Posted: 2025-04-18
• Last Update Posted: 2025-04-18
• Study Start: 2025-05-01
• Primary Completion: 2026-03-01
• Study Completion: 2026-05-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• ASA 1 to ASA 2 18 to 60 years

Exclusion Criteria

• patient refusal Significant neurological , psychiatric or neuromascular disease Drug abuse Pregnant or lactating women Suspected coagulopathy Morbid obesity Known allergy to some medications Septicaemia and local infection at block site

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Erector spinae plane block group	Sonographic guided Erector spinae plane block	-
Conventional analgesia group	Intravenous opioid	-

Primary Outcome Measures

Name	Time	Method
Reduction of postoperative pain	1 year	VAS score for pain measurement