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Comparison of use of bupivacaine and ropivacaine with use of ultrasound in erector spinae block for poster operative pain relief in spine surgeries

Comparison of Bupivacaine and Ropivacaine in Ultrasound-guided bilateral erector spine plane block for post-operative analgesia in lumbar spine surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054776
Enrollment
70
Registered
2023-07-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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: Ultrasound-guided bilateral erector spinae plane block for post operative analgesia in lumbar spine surgery: Use of 0.25% Bupivacaine for erector spinae plane block Control Intervention

Sponsors

ABVIMS and Dr.RML Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA Grade I and II,Patients posted for lumbar spine surgery

Exclusion criteria

Exclusion criteria: Patients not consenting to the procedure Local infection at the block site Pre- existing coagulation disorders Allergy to local anesthetics (prior test dosing with Bupivacaine and ropivacaine will be given)

Design outcomes

Primary

MeasureTime frame
Duration of postoperative analgesia,time between institution of block and requirement of first rescue analgesiaTimepoint: Before shifting to PACU Immediately after shifting to PACU 30 minutes 1st hour 1.5 hour 2nd hour 4th hour 6th hour 8th hour 10th hour 12 th hour—

Secondary

MeasureTime frame
Postoperative hemodynamic parameters Post operative nausea vomiting and any other adverse effectsTimepoint: Before shifting to PACU Immediately after shifting to PACU 30 minutes 1st hour 1.5 hour 2nd hour 4th hour 6th hour 8th hour 10th hour 12 th hour—

Countries

India

Contacts

Public ContactYAMUNA KRISHNAN

ABVIMS and Dr. RML Hospital

alkagupta_rml@yahoo.co.in9871653335

Outcome results

None listed

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