Skip to content

A study to compare the efficacy of erector spinae block and quadratus lumborum block for pain management in kidney transplant donors after sugery.

Efficacy of erector spinae block Vs quadratus lumborum block type II in renal transplant donors for post-operative analgesia.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041599
Enrollment
75
Registered
2022-04-04
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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: Erector spinae block: In addition to the standard anlalgesia care which includes paracetamol 1 gram, i.v. ketorolac (0.5 mg/kg) for postoperative pain management and ondansetron 4 mg at

Sponsors

Sishir Siwakoti
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Laparoscopic donor nephrectomy patients ASA class I and II

Exclusion criteria

Exclusion criteria: Patient unacceptance. Local infection of the skin where block is to be given. History of allergy to the local anesthetic agents used in this study. Patients with history of coagulation disorder or if patient is under any anticoagulant drugs. End-stage organ and system failure, severe pulmonary and/or cardiovascular problem. Substance addiction or known psychiatric or mental problems.

Design outcomes

Primary

MeasureTime frame
The primary outcome of this trial is cumulative morphine consumption over 24 hours Timepoint: 1, 3, 6, 12 and 24 hours after surgery

Secondary

MeasureTime frame
Evaluation of pain: NRS score for pain in the first postoperative 24h. Timepoint: 1, 3, 6, 12 and 24 hours after surgery. ;Hemodynamic profile of the patient, namely heart rate and Mean Arterial pressureTimepoint: 1, 3, 6, 12 and 24 hours after surgery. ;Intervention-related complications including hematoma, organ injuries, and lower extremity weakness, vascular puncture, kidney injury in the interventional group. Timepoint: 1, 3, 6, 12 and 24 hours after surgery.

Countries

India

Contacts

Public ContactDr Sameer Sethi

PGIMER

sameersethi29@gmail.com9317851002

Outcome results

None listed

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