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Recruiting NCT06852378

Iliopsoas Nerve Block and Femoral Nerve Block in Hip Fracture Surgeries

Observational Iliopsoas Nerve Block Femoral Nerve Block Hip Fracture Surgeries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Iliopsoas nerve block, Femoral nerve block.
Who it may be relevant to
Registry conditions: Iliopsoas Nerve Block, Femoral Nerve Block, Hip Fracture Surgeries. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison Between Iliopsoas Nerve Block and Femoral Nerve Block in Hip Fracture Surgeries

Overview

This study aims to compare iliopsoas nerve Block (IPB) to femoral nerve block (FNB) regarding pain control, patient satisfaction, and early ambulation in patients undergoing hip fracture surgeries

Detailed description

Hip fractures are among the most frequent fractures seen in the emergency department and orthopedic trauma teams. The terms hip fracture and neck of femur fracture are used synonymously. Both terms describe a proximal femur fracture between the femoral head and 5 cm distal to the lesser trochanter.

Iliopsoas nerve Block (IPB) is a promising motor-sparing analgesic technique that selectively targets the sensory branches of the hip joint originating from the femoral nerve and accessory obturator nerve, sparing the motor supply of quadriceps muscles.

A femoral nerve block (FNB) is a simple nerve block that can be performed easily without or under ultrasound guidance. Under ultrasound guidance, the femoral artery and femoral nerve were identified clearly, and a needle was inserted using an in-plane approach from the lateral to the medial direction. Once the needle tip's position was confirmed, 10 ml of 0.5% bupivacaine was injected adjacent to the femoral nerve.

Interventions

  • Drug Iliopsoas nerve block
    Patients will receive an Iliopsoas nerve block using 10 ml of bupivacaine 0.5%.
  • Drug Femoral nerve block
    Patients will receive femoral nerve block using 10 ml of bupivacaine 0.5%.

Primary outcome measures

  • Degree of pain [Time frame: 24 hours postoperatively]
Secondary outcome measures (5)
  • Total opioids consumption [Time frame: 24 hours postoperatively]
  • Assessment of quadriceps strength [Time frame: 24 hours postoperatively]
  • Time of ambulation [Time frame: 24 hours postoperatively]
  • Patients' satisfaction [Time frame: 24 hours postoperatively]
  • Incidence of complications [Time frame: 24 hours postoperatively]

Eligibility criteria

Inclusion criteria

  • Age from 18 to 65 years.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status I and II.
  • Patients who are scheduled for elective surgical correction of hip fracture either through open fracture internal fixation (ORIF), partial hip arthroplasty or total hip arthroplasty.

Exclusion criteria

  • Refusal to participate.
  • Coagulopathy.
  • Patients with a history of drug allergies to study drugs.
  • Inability to cooperate.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Egypt · 1 center
  • Ain Shams University — Cairo

Identifiers

NCT: NCT06852378 · FMASU MD38/2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗