Patients undergoing femur fracture surgery will be divided into two groups and given ultrasound guided supra inguinal fascia iliaca block using bupivacaine 0.25% or bupivacaine 0.125% to compare their effect in controlling pain.

Ultrasound guided Supra inguinal fascia ilaica block for post operative analgesia in patients undergoing femur fracture sugery:A randomised control trail study comparing bupivacaine(0.25%) and bupivacaine(0.125%) - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/05/087569

Enrollment

Registered

2025-05-26

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

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

Conditions

Health Condition 1: V299- Motorcycle rider (driver) (passenger) injured in unspecified traffic accident

Interventions

Intervention1: 20 ml Bupivacaine 0.250%: local anesthetic drug used for regional blockade. Control Intervention1: 20 ml Bupivacaine 0.125%: Low concentration of local anesthetic drug used for regional

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA Grade 1-2, 2.Patients who are between 18-50 years posted for elective surgery for femur fracture under spinal anesthesia

Exclusion criteria

Exclusion criteria: 1. ASA Grade 3-5 2. Patients who refuses to participate in the study. 3. History of anaphylaxis to local anesthetic agents. 4. Deranged coagulation profile, 5.Presence of infection at the site of block, 6.Neurological deficits like paresis or paraplegia of the lower limb, 7.Motor power less than 5/5.

Design outcomes

Primary

Measure	Time frame
1.Less consumption of opioids. 2.Lower VAS score pre and post block 3.comfortable positioning for patients undergoing neuraxial blockade.Timepoint: 1.VAS score pre block(baseline) 2.VAS score post block(20 minutes) 3.Hemodynamic parameters after subarachnoid blockade 0 minutes 3 minutes 10 minutes 30 minutes 1 hour 2 hours 3 hours	—

Secondary

Measure	Time frame
post op VAS score less hemodynamic fluctuations less side effectsTimepoint: 6 hours 12 hours 18 hours 24 hours	—

Countries

India

Contacts

Public ContactDR Sourabh Kumar

Rajendra Institute of Medical Sciences ,Ranchi

ekramrims@yahoo.co.in9431101186

Outcome results

None listed

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