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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/12/038662
Enrollment
60
Registered
2021-12-15
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Group B:Lumbar Erector Spinae Plane block with Inj Bupivacaine 0.25% 35 ml: The 4th lumbar vertebral level will be determined using the conventional method. The convex USG transducer wi

Sponsors

Bangalore Baptist Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patient of ASA(American Society of Anesthesiologist) physical status 1,2,3 Elective and emergency femur surgeries

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
1)Efficacy of post operative analgesia(till 24hrs 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 analgesiaTimepoint: 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

MeasureTime frame
1)Incidence of any adverse events 2)Assessment of motor power in both groupsTimepoint: within first 24 hours

Countries

India

Contacts

Public ContactDr Laji Abraham Samuel

Bangalore Baptist Hospital

Drlajisamuel@gmail.com8317397242

Outcome results

None listed

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