FindTrial
Sign In

Comparison of two ultrasound-guided nerve blocks for pain relief after laparoscopic kidney surgery.

Comparison of analgesic efficacy between modified external oblique plane block and erector spinae plane block in adult patients undergoing laparoscopic renal surgeries: a randomised controlled trial. - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/11/097202
Enrollment
66
Registered
2025-11-11
Start date
Unknown
Completion date
Unknown
Last updated
2025-11-17

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: modified external oblique plane block and erector spinae plane block: Comparison of analgesic efficacy between modified external oblique plane block and erector spinae plane block in ad

Sponsors

AIIMS PATNA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adult patients (18-70 years) 2.Patients of American Society of Anaesthesiologists Physical Status (ASA-PS) I or II scheduled for laparoscopic renal surgeries (Nephrectomy, Pyeloplasty, Pyelolithotomy). 3.Patients willing to give consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1.History of allergy to any of the study drug 2.Body Mass Index less than18 or more than 35 kg per meter square. 3.Coagulopathy (INR more than 1.5 and(or)or platelet count less than 70,000 per ml) 4.Local infection 5.History of chronic pain 6.History of regular opioid use 7.Inability to comprehend NRS

Design outcomes

Primary

MeasureTime frame
To compare the time to first rescue analgesia between MEOP block and ESP block in adult patients undergoing laparoscopic renal surgeries.Timepoint: Within 24 hours of postoperative period.—

Secondary

MeasureTime frame
Pain intensity measured using the Numerical Rating Scale (NRS)Timepoint: 1,24,8,12 and 24 hours.;Total opioid consumptionTimepoint: Within 24 hours of postoperative period;Intra operative fentanyl consumptionTimepoint: Through the duration of the surgery—

Countries

India

Contacts

Public ContactDr Rajnish Kumar

AIIMS PATNA

drrajnishkumar@aiimspatna.org7783865337

Outcome results

None listed

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