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A clinical study to know the usefulness of Nerve block for pain management post surgery under help of ultrasound machine in patient undergoing PCNL Surgery

A Prospective randomized double blinded controlled study based on usefulness of Erector spinae block under ultrasound guidance versus control in patient undergoing PCNL Surgery. - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065654
Enrollment
60
Registered
2024-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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: Erector Spinae Block using 110 mm sonotap needle. 20 ml of 0.25 percent of Bupivacaine at T 12 and T 10 level, 10 ml at each level, post operative before extubatio

Sponsors

Sri narayani hospital and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.American society of Anesthesiologist I and II 2.Patient with BMI more than 35

Exclusion criteria

Exclusion criteria: 1.patient with excessive bleeding 2.patients having supracostal puncture. 3.significant residual stone more than 1 cm and need for second look. 4.solitary kidney 5.dermal infection in the injection site 6.contrast and drug allery 7.Body mass index more than 35 7.Surgery lasting more than 180 minutes.

Design outcomes

Primary

MeasureTime frame
Favourable outcome is expected for ultrasound guided ESP Block in comparison to control group.Timepoint: 1 hour, 2 hour, 3 hour, 4 hour,5 hour, 6 hour, 10 hour, 14 hour, 18 hour, 24 hour.

Secondary

MeasureTime frame
Total analgesic requirement in 24 hour and Postoperative opioid consumption.Timepoint: 1 hour, 2 hour, 3 hour, 4 hour, 5 hour, 6 hour, 10 hour, 14 hour, 18 hour, 24 hour.

Countries

India

Contacts

Public ContactDr Anagha Vinod

Sri Narayani Hospital and Research Centrere

seekala@gmail.com9626888412

Outcome results

None listed

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