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Clinical Trials/CTRI/2022/08/045117
CTRI/2022/08/045117Not yet recruitingPhase 4

Comparison Between Relative Efficacy Of Erector Spinae Plane Block And Caudal Epidural Injection For Early Postoperative Analgesia In Patients Undergoing Lumbar Spine Fusion Surgery - A prospective Randomized Study

Ganga Medical Centre And Hospital Pvt Ltd1 site in 1 country81 target enrollmentStarted: January 10, 2022Last updated:
Conditions

Trial Snapshot

Phase
Phase 4
Status
Not yet recruiting
Enrollment
81
Locations
1
Primary Endpoint
Assessment Of NRS Score

Study Overview

Brief Summary

Randomized Controlled study to Compare the relative efficacy of erector spinae plain block and caudal epidural injection for early post operative analgesia in patients undergoing single level lumbar fusion surgery.

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Participant, Investigator and Outcome Assessor Blinded

Eligibility Criteria

Ages
20.00 Year(s) to 70.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Single Level Lumbar Fusion Surgery Patients.

Exclusion Criteria

  • •Spinal Infections tumor and trauma Patients With Neurological Deficits Previous Spine Surgery Patients With Dural Tear.

Outcomes

Primary Outcomes

Assessment Of NRS Score

Time Frame: To Assess Postoperative | Vas/Pain Score at 2hour, 4 hour, 8 hour, 12 hour, 24 hour. and 48 hours

Secondary Outcomes

  • Anti Emetic Requirement(PONV scale)

Investigators

Sponsor Class
Research institution and hospital

Study Sites (1)

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