Erector Spinae Block vs Conventional Analgesia for Postoperative Analgesia in PCNL
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Sonographic guided Erector spinae plane block, Intravenous opioid.
- Who it may be relevant to
- Registry conditions: Percutaneous Nephrolithotomy (PCNL). Basic parameters: 18 years — 60 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Sonographic Guided Erector Spinae Plane Block Versus Conventional Analgesia After Percutaneous Nephrolithotomy a Comparative Randomized Study
Overview
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
Interventions
- Procedure 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 - Drug Intravenous opioid
0.1 mg/kg morphine intravenous pre operative
Primary outcome measures
- Reduction of postoperative pain [Time frame: 1 year]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06935006 · Soh-Med-22-06-35