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Clinical Trials/CTRI/2021/12/038662
CTRI/2021/12/038662Not yet recruitingNot Applicable

Comparison of ultrasound guided Lumbar Erector Spinae Plane block versus Ultrasound guided Fascia Iliaca Compartment block for postoperative analgesia after femoral surgeries-A randamized control study

Bangalore Baptist Hospital1 site in 1 country60 target enrollmentStarted: December 23, 2021Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
60
Locations
1
Primary Endpoint
1)Efficacy of post operative analgesia(till 24hrs after shifting out from OT) as evaluated by numerical rating scale

Study Overview

Brief Summary

This study aims to compare the effects of ultrasound-guided Lumbar erector spinae plane block versus ultrasound-guided Fascia iliaca Compartment block for postoperative analgesia following femur surgeries. The two groups will be assessed in terms of efficacy of analgesia, as measured by a standardized pain assessment score. The requirement of rescue analgesia in the first 24hours and proportions of patients who requires will also be assessed. Nausea , vomiting and  residual motor weakness in both the groups will be recorded. We want to know if the Lumbar Erector Spinae  block provides as good or better postoperative analgesia than the Fascia Iliaca Compartment block as part of a multimodal analgesia for femoral surgeries.

Study Design

Study Type
Interventional
Allocation
Computer generated randomization
Masking
Open Label

Eligibility Criteria

Ages
18.00 Year(s) to 80.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • patient of ASA(American Society of Anesthesiologist) physical status 1,2,3 Elective and emergency femur surgeries.

Exclusion Criteria

  • Refusal of consent for study Patient with bleeding or coagulation abnormalities or on therapeutic anticoagulants medications Infection or injury at the injection site Patients with significant preexisting neurological deficits, both central and peripheral Acute polytrauma cases Patient with history of allergy to local anesthetic/Diclofenac Hemodynamically unstable patients or those requiring postoperative ventilation.

Outcomes

Primary Outcomes

1)Efficacy of post operative analgesia(till 24hrs after shifting out from OT) as evaluated by numerical rating scale

Time Frame: 1)Efficacy of post operative analgesia(till 24 hrs after shifting out from OT) as evaluated by numerical rating scale | 2)Total rescue analgesia use(till 24 hrs after shifting out from OT) | 3)Proportion of patient who requires rescue analgesia

2)Total rescue analgesia use(till 24 hrs after shifting out from OT)

Time Frame: 1)Efficacy of post operative analgesia(till 24 hrs after shifting out from OT) as evaluated by numerical rating scale | 2)Total rescue analgesia use(till 24 hrs after shifting out from OT) | 3)Proportion of patient who requires rescue analgesia

3)Proportion of patient who requires rescue analgesia

Time Frame: 1)Efficacy of post operative analgesia(till 24 hrs after shifting out from OT) as evaluated by numerical rating scale | 2)Total rescue analgesia use(till 24 hrs after shifting out from OT) | 3)Proportion of patient who requires rescue analgesia

Secondary Outcomes

  • 1)Incidence of any adverse events(2)Assessment of motor power in both groups)

Investigators

Sponsor Class
Research institution and hospital

Study Sites (1)

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