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Comparison between Femoral Nerve Block and Fascia Iliaca Compartment Block for reducing pain associated with positioning for spinal anaesthesia in proximal femur fracture surgery.

A Randomised Comparative Study Of Ultrasound Guided Femoral Nerve Block Vs Fascia Iliaca Compartment Block For Reducing Pain Associated With Positioning For Spinal Anesthesia In Patients With Proximal Femur Fracture At SMS Hospital, Jaipur.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043059
Enrollment
86
Registered
2022-06-07
Start date
Unknown
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: 43 Patients will receive Ultrasound guided Fascia Iliaca Compartment Block with 30ml of 0.25% Bupivacaine.: Effect will be checked by pin prick sensation on anterior part of thigh. VAS

Sponsors

Sawai Man Singh Medical College Jaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient undergoing elective surgery for proximal femur fracture unable to sit for SAB due to severe pain.(VAS >7) 2.Patients consenting to participate. 3.Adult patients aged 18-80 Years. 4.Patients belonging to American Society Of Anesthesiologists(ASA) grade I, II and III. 5.Weight 40-80 kgs.

Exclusion criteria

Exclusion criteria: 1.Patients with psychiatric illness, anxious, agitated. 2.Patients with peripheral sensorineural deficit. 3.Patients allergic to local anesthetics. 4.Patients on anticoagulant therapy. 5.Infection at block site. 6.Patients with multiple trauma. 7.Patients with suspected compartment syndrome in lower limbs. 8.Patients on analgesia within 8 hours before performing nerve block. 9.Block failure cases.

Design outcomes

Primary

MeasureTime frame
To determine the change in VAS score from baseline to post induction at different time intervals. Timepoint: To determine the change in VAS score from baseline to post induction at different time intervals maximum up to 15 minutes (until the VAS score is less than 3) in both groups.—

Secondary

MeasureTime frame
1.To estimate Anesthesiologist satisfaction score. 2.To determine the difference in mean time of first rescue analgesia in both groups by using VAS score. 3.To determine the difference in mean dose of analgesia required in both groups. 4.To determine the change in the haemodynamic parameters (HR,SBP,DBP,MAP and SpO2 )in both groups. 5.To observe side effect if any. Timepoint: 1.To estimate Anesthesiologist satisfaction score. 2.To determine the difference in mean time of first rescue analgesia in both groups by using VAS score. 3.To determine the difference in mean dose of analgesia required for 24 hours in both groups. 4.To determine the change in the haemodynamic parameters (HR,SBP,DBP,MAP and SpO2 )in both groups. 5.To observe side effect if any.—

Countries

India

Contacts

Public ContactDr Kanupriya

Sawai Man Singh Medical College, Jaipur

drmamtakhandelwal@gmail.com9929338174

Outcome results

None listed

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