Comparison of two types of nerve blocks to reduce pain after renal surgeries.

A study to compare and evaluate the analgesic efficacy of erector spinae block and anterior quadratus lumborum block using levobupivacaine in renal surgeries. - Nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/09/095506

Enrollment

Registered

2025-09-30

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: N29- Other disorders of kidney and ureter in diseases classified elsewhere Health Condition 2: 8- Other Procedures

Interventions

Intervention1: Erector Spinae Plane Block: Group E -patient will receive a local anaesthetic of 25ml 0.25% of injection levobupivacaine 25 min before surgery. These patients will receive ultrasound gu

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 to 3 Both Gender Elective Renal Surgeries under General Anaesthesia Age 18 to 60 Patients able to understand and rate their pain according to visual Analouge Scale Patient giving consent for block

Exclusion criteria

Exclusion criteria: Pregnant females Patients having history of drug allergy to levobupivacaine Patient having history of significiant respiratory or cardiovascular or hepatic or endocrine and psychiatry disease Patient not giving consent for performing block BMI more than 35 per metre square

Design outcomes

Primary

Measure	Time frame
To compare the efficacy of erector spinae plane block and anterior quadratus lumborum block using levobupivacaine in renal surgeriesTimepoint: 24 hours post operative period	—

Secondary

Measure	Time frame
To record the timing of first rescue analgesia and total requirement of rescue analgesia To measure incidence of complications such as Hematoma Vomiting HypotensionTimepoint: ;Time of requirement for first rescue analgesia in post operative period. Total amount of rescue analgesia consumed in first 24 hours To measure incidence of complications such as Hematoma Vomiting Hypotension Timepoint: 24 hours post operative peroid	—

Measure

Time frame

To record the timing of first rescue analgesia and total requirement of rescue analgesia To measure incidence of complications such as Hematoma Vomiting HypotensionTimepoint: ;Time of requirement for first rescue analgesia in post operative period. Total amount of rescue analgesia consumed in first 24 hours To measure incidence of complications such as Hematoma Vomiting Hypotension Timepoint: 24 hours post operative peroid

—

Countries

India

Contacts

Public ContactDr Shiv Kumar

School of medical sciences and research

Shiv.singh@sharda.ac.in9650943359

Outcome results

None listed

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