A clinical trial to compare the effect of drug ropivacaine when given via two routes, erector spinae plane block and peritubal local infiltration for post operative pain management in patients undergoing percutaneous nephrolithotomy surgery.

Comparison Of Efficacy Of Ultrasound Guided Erector Spinae Plane Block Versus Peritubal Infiltration Of Local Anaesthetic For Post Operative Analgesia In Percutaneous Nephrolithotomy Under General Anaesthesia - nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/08/056925

Enrollment

Registered

2023-08-25

Start date

Unknown

Completion date

Unknown

Last updated

2023-09-18

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

Conditions

Health Condition 1: N200- Calculus of kidney Health Condition 2: N00-N99- Diseases of the genitourinary system

Interventions

Intervention1: Ultrasound Guided Erector Spinae Plane Block with 0.25% Ropivacaine 20mL: • In the operation theatre, standard monitors will be attached such as an electrocardiograph, non invasive bloo

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age (18-65) years 2. All genders 3. Patients with ASA grade I/II 4. Patients undergoing PCNL surgery under GA

Exclusion criteria

Exclusion criteria: 1. Infection at local site 2. H/o drug abuse, psychiatric disorder, chronic pain 3. Coagulation abnormalities 4. Pregnant or lactating females 5. Refusal for consent of peripheral nerve block 6. History of drug allergy.

Design outcomes

Primary

Measure	Time frame
To compare the post operative pain score of two groups (Erector Spinae Plane Block & Peritubal infiltration of LA) using Visual Analogue Scale (VAS)Timepoint: Post-operative pain score monitoring by VAS score at 30min, 60min, 2h, 4h, 8h, 12h, 16h, 20h & 24hour.	—

Secondary

Measure	Time frame
1) To compare time to first rescue analgesia in both groups. 2) To compare total consumption of analgesics in first 24 hours post operatively. 3) To compare patient satisfaction in both groups. 4) Comparison of occurrence of any complication in either group.Timepoint: first 24 hours post operatively	—

Countries

India

Contacts

Public ContactDr Astha Agarwal

Mahatma Gandhi Medical College and Hospital

khayyammoin@yahoo.com9468964148

Outcome results

None listed

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