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Erector Spinae Block vs Conventional Analgesia for Postoperative Analgesia in PCNL

S

Sohag University

Status

Not yet enrolling

Conditions

Percutaneous Nephrolithotomy (PCNL)

Treatments

Procedure: Sonographic guided Erector spinae plane block
Drug: Intravenous opioid

Study type

Interventional

Funder types

Other

Identifiers

NCT06935006
Soh-Med-22-06-35

Details and patient eligibility

About

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

Enrollment

50 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

50 participants in 2 patient groups

Erector spinae plane block group
Active Comparator group
Treatment:
Procedure: Sonographic guided Erector spinae plane block
Conventional analgesia group
Active Comparator group
Treatment:
Drug: Intravenous opioid

Trial contacts and locations

0

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Central trial contact

Fawzy Abbas, Assistant professor; Ahmed Mahmoud Azmy, Assistant lecturer

Data sourced from clinicaltrials.gov

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