A trial to compare pain control after PCNL surgery between Erector Spinae muscle plane block and renal injection through the nephrostomy tube with 0.25% injection Levobupivacaine administered randomly.

A study to compare postoperative analgesic outcome between Erector Spinae plane block and renal peritubal infiltration with 0.25% Levobupivacaine in patients undergoing percutaneous nephrolithotomy - An observer blind randomized trial.

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2022/11/047001

Enrollment

Registered

2022-11-03

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: - Health Condition 2: N200- Calculus of kidney

Interventions

Intervention1: Erector Spinae plane block with 20 ml of 0.25% Levobupivacaine: After PCNL surgery patient still in prone position will be given landmark guided Erector spinae plane block at T9 transv

Eligibility

Inclusion criteria

Inclusion criteria: Patients with age between 18 to 65 years and of American Society of Anesthesiologist (ASA) category 1 or 2 of both sexes, who give informed consent to participate in the study and who undergo PCNL surgery in our institute during the study period.patient having single access PCNL.

Exclusion criteria

Exclusion criteria: ) Significant residual stones ( >1 cm in diameter) after surgery and the need for a second look (b) Bleeding diathesis (c) A solitary kidney; (f) Routine antidepressant, corticosteroid, pain medication, or anticonvulsant usage, (g) A mental state preventing the effective use of VAS score.

Design outcomes

Primary

Measure	Time frame
Primary outcome-Time to first rescue analgesia (hrs) ie, time from successful completion of block till first administration of rescue analgesic.Timepoint: Primary outcome-Time to first rescue analgesia (hrs) ie, time from successful completion of block till first administration of rescue analgesic.	—

Secondary

Measure	Time frame
VAS score at time intervals, total rescue analgesic required, SBP,DBP, heart rate at intervals, adverse effectsTimepoint: Assessment at intervals 1 ,2,4,6,12,18 and 24 hours postoperatively.	—

Countries

India

Contacts

Public ContactDr Anjan Chattopadhyay

IPGMER and SSKM Hospital Kolkata.

anjan.chat@gmail.com9831257338

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026