Erector Spinae Block vs Conventional Analgesia for Postoperative Analgesia in PCNL

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-05-01

Study Completion Date

2026-05-01

Brief Summary

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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

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Detailed Description

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Conditions

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Percutaneous Nephrolithotomy (PCNL)

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Erector spinae plane block group

Group Type ACTIVE_COMPARATOR

Sonographic guided Erector spinae plane block

Intervention Type PROCEDURE

Ultrasound guided plane block using 20 ml of 0.25% bupivacaine at the level of transverse process of T8

Conventional analgesia group

Group Type ACTIVE_COMPARATOR

Intravenous opioid

Intervention Type DRUG

0.1 mg/kg morphine intravenous pre operative

Interventions

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Sonographic guided Erector spinae plane block

Ultrasound guided plane block using 20 ml of 0.25% bupivacaine at the level of transverse process of T8

Intervention Type PROCEDURE

Intravenous opioid

0.1 mg/kg morphine intravenous pre operative

Intervention Type DRUG

Eligibility Criteria

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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

Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No