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Study to compare between 2 types of nerve block to for relieve pain after bone surgery.

Not yet recruiting
Conditions
Diseases of the musculoskeletal system and connective tissue, (2) ICD-10 Condition: O||Medical and Surgical,
Registration Number
CTRI/2021/12/038662
Lead Sponsor
Bangalore Baptist Hospital
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
60
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.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1)Efficacy of post operative analgesia(till 24hrs after shifting out from OT) as evaluated by numerical rating scale1)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)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 analgesia1)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 Outcome Measures
NameTimeMethod
1)Incidence of any adverse events2)Assessment of motor power in both groups

Trial Locations

Locations (1)

Bangalore Baptist Hospital

🇮🇳

Bangalore, KARNATAKA, India

Bangalore Baptist Hospital
🇮🇳Bangalore, KARNATAKA, India
RANJITHA K V
Principal investigator
9741614845
ranjithakv65@gmail.com

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