Erector spinae plane block along with general anaesthesia in patients posted for percutaneous nephrolithotomy surgery for assessing post-operative quality of recovery

Erector spinae plane block supplementation to general anaesthesia in percutaneous nephrolithotomy surgery for post-operative quality of recovery - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/09/094943

Enrollment

Registered

2025-09-16

Start date

Unknown

Completion date

Unknown

Last updated

2025-10-13

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Erector spinae plane block supplementation to general anaesthesia: Patients posted for PCNL surgery will be given erector spinae plane block using 20ml 0.25% levobupivacaine between the

Eligibility

Inclusion criteria

Inclusion criteria: ASA class I and II Patients posted for elective percutaneous nephrolithotomy surgery

Exclusion criteria

Exclusion criteria: Patient not giving consent Age less than 18 years and more than 60 years ASA class III and IV Allergic to levobupivacaine Pregnant and lactating female Patient with any spinal deformity

Design outcomes

Primary

Measure	Time frame
To assess the effect of erector spinae plane block supplementation to general anaesthesia on postoperative analgesia and time of first opioid consumptionTimepoint: 24 hours	—

Secondary

Measure	Time frame
To compare the postoperative quality of recovery in the two groups with the help of QoR 15 scoreTimepoint: At the time of discharge	—

Countries

India

Contacts

Public ContactDr Anupam Pandey

Peoples College of Medical Sciences and Research Centre

docanshu07@rediffmail.com8889480540

Outcome results

None listed

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