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Comparison of effect of erector spinae plane block versus transmuscular quadratus lumborum block on pain relief after laparoscopic or robot assisted renal surgeries

Comparison of analgesic efficacy of ultrasound guided Erector spinae plane block versus Transmuscular Quadratus lumborum block in patients undergoing laparoscopic or robot assisted renal surgeries a double blind randomised controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/082345
Enrollment
64
Registered
2025-03-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-07

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: Erector Spinae Plane block is an interfacial nerve block which provides both visceral and somatic analgesia. This will be administered before general anaesth

Sponsors

Dhruvika Dabi
Lead Sponsor
Department of Anaesthesiology Pain Medicine and Critical Care
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age: 18 years and above 2. ASA I-III 3. Patients scheduled for laparoscopic or robot assisted renal surgeries

Exclusion criteria

Exclusion criteria: 1. Allergy to local anesthetics 2. Inability to communicate 3. Chronic pain or recent acute pain 4. Severe liver or renal dysfunction 5. Long term use of analgesic or sedatives 6. Refusal to give consent 7. BMI greater than 35kg/m2

Design outcomes

Primary

MeasureTime frame
Cumulative PCA fentanyl consumption within 24 hrs after surgeryTimepoint: at 24 hrs after surgery

Secondary

MeasureTime frame
1. NRS at rest on coughing at 0.5,1,2,4,8,12 and 24 hours postoperatively  2. Time to activation of PCA 3. Use of rescue analgesia  4. Qor-15 score at 24 and 48 hrs postoperatively 5. Length of hospital stay 6. Time to mobilisation to chair from T0( Time of arrival to PACU) 7. Time to first walk (10 mtrs) from T0 (Time of arrival to PACU) 8. Incidence and severity of opioid-related adverse effects such as nausea and vomiting, respiratory depression, pruritis and sedation 9. Subjective sleep quality on the night of surgery 10. Baseline and 24 hrs postoperative CRP levelsTimepoint: 0.5 hour, 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 24 hours, 48 hours

Countries

India

Contacts

Public ContactDhruvika Dabi

All India Institute of Medical Sciences

vimirewari@gmail.com9818304880

Outcome results

None listed

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