MedPath

Comparative study between femoral nerve block versus pericapsular nerve group block for pain in proximal femoral fractures during anesthesia positioning

Not yet recruiting
Conditions
Medical and Surgical,
Registration Number
CTRI/2021/11/038334
Lead Sponsor
Sree Balaji Medical College and hospital
Brief Summary

This is a comparative study, to be done in total number of 50 patients who are undergoing proximal femur fracture surgeries at Department of Anaesthesiology PM &CC,Sree Balaji medical College and Hospital, Chennai.

After confirming to the inclusion and exclusion criteria, patients will be selected consecutively and Assigned alternatively to either of the two groups. The first group shall undergo USG guided pericapsular nerve group block and the second group shall undergo USG  guided femoral nerve block with 10ml of 2% lignocaine plus 0.5% bupivacaine. Both the groups The procedure under USG guidance 20 minutes prior to positioning the patient for spinal anaesthesia. The quality of patients positioning during the spinal anesthesia was graded according to the scale( 1- satisfactory,2- good 3-optimal) and was recorded. Pain status will be assessed by numerical rating pain score before, after and while positioning the patient for spinal anesthesia. The hemodynamic status of the patients will be recorded throughout the whole process.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria
  • All patients undergoing lower limb surgery at Sree Balaji Medical College and Hospital 1. ASA grade.
  • l, ll, lll 2. Patients posted for proximal femoral fracture 3. Patients posted for elective surgeries.
Exclusion Criteria
  • Patient refusal 2.
  • ASA grade lV 3.
  • Morbidly obese patient 4.
  • Known case of hypersensitivity reaction to local anaesthetics.
  • Bleeding diathesis, peripheral neuropathy and psychiatric disorder.
  • Local infection at the site of puncture.
  • Patients with polytrauma.
  • Previous femoral bypass surgeries.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To find which block patience provides more analgesia, haemodynamic status and ease of the patient while positioning the patient for spinal anaesthesia.Till positioning of the patient for spinal anesthesia
Secondary Outcome Measures
NameTimeMethod
Comparing the efficacy of two blocksFrom the time of performing the block Till positioning of the patient

Trial Locations

Locations (1)

Sree Balaji medical College and Hospital

🇮🇳

Chennai, TAMIL NADU, India

Sree Balaji medical College and Hospital
🇮🇳Chennai, TAMIL NADU, India
DrAkash
Principal investigator
9043739347
akashyadhu@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.