Erector Spinae Block vs Conventional Analgesia for Postoperative Analgesia in PCNL

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorSohag University

About this trial

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

Eligibility criteria

Qualifiers

ASA 1 to ASA 2 18 to 60 years

Disqualifiers

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

Treatments tested in this trial

  • Sonographic guided Erector spinae plane block
  • Intravenous opioid

Treatment groups

50 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators