Comparison between Femoral Nerve Block and Fascia Iliaca Compartment Block for reducing pain associated with positioning for spinal anaesthesia in proximal femur fracture surgery.
- Conditions
- Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system
- Registration Number
- CTRI/2022/06/043059
- Lead Sponsor
- Sawai Man Singh Medical College Jaipur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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.
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the change in VAS score from baseline to post induction at different time intervals. <br/ ><br> <br/ ><br>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)Â in both groups. <br/ ><br> <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.To estimate Anesthesiologist satisfaction score. <br/ ><br>2.To determine the difference in mean time of first rescue analgesia in both groups by using VAS score. <br/ ><br>3.To determine the difference in mean dose of analgesia required in both groups. <br/ ><br>4.To determine the change in the haemodynamic parameters (HR,SBP,DBP,MAP and SpO2 )in both groups. <br/ ><br>5.To observe side effect if any. <br/ ><br>Timepoint: 1.To estimate Anesthesiologist satisfaction score. <br/ ><br>2.To determine the difference in mean time of first rescue analgesia in both groups by using VAS score. <br/ ><br>3.To determine the difference in mean dose of analgesia required for 24 hours in both groups. <br/ ><br>4.To determine the change in the haemodynamic parameters (HR,SBP,DBP,MAP and SpO2 )in both groups. <br/ ><br>5.To observe side effect if any. <br/ ><br>