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Erector Spinae Plane Block(Nerve block) for pain relief after percutaneous nephrolithotomy surgery

Ultrasound Guided Erector Spinae Plane Block for Postoperative Analgesia in Patients undergoing Percutaneous Nephrolithotomy – A Double-blinded, Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/017051
Enrollment
60
Registered
2019-01-11
Start date
Unknown
Completion date
Unknown
Last updated
2023-08-21

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

Interventions

Intervention1: General anaesthesia with Unilateral Erector Spinae Plane block with 20 ml of 0.5% Ropivacaine: Erector Spinae Plane block is a interfascial nerve block which provides both visceral and

Sponsors

Vimi Rewari
Lead Sponsor
Department of AnaesthesiologyPain Medicine and Critical Care
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade I -III patients 2.Patients scheduled to undergo elective percutaneous nephrolithotomy surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: 1.Patient refusal to participate 2.BMI = 35 kg/m2 3.Known hypersensitivity to local anaesthetic and opioids 4.Patient having infection at the site of block 5.Patient having spinal deformities and previous history of spine surgery 6.History of coagulopathy and on anticoagulant therapy 7.Patients with history of psychiatric illness and patients who are unable to comprehend instructions

Design outcomes

Primary

MeasureTime frame
1.Total postoperative morphine consumption at 24 hoursTimepoint: 24 hours postoperatively

Secondary

MeasureTime frame
1. Total intraoperative fentanyl requirement 2. Time to activation of IV morphine PCA pump postoperatively 3. Postoperative pain at rest and on coughing as assessed by VAS scale at 1hour, 2hours, 4 hours, 6hours, 12hours and 24hours postoperatively 4. Incidence of opioid-related adverse effects such as nausea and vomiting, respiratory depression and sedation 5. Requirement of rescue analgesics 6. Patient satisfaction score Timepoint: 1hour, 2hours, 4 hours, 6hours, 12hours and 24hours postoperatively

Countries

India

Contacts

Public ContactYokasekar V

AIl India Institute of Medical Sciences

vimirewari@gmail.com9818304880

Outcome results

None listed

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