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Peri-Capsular Nerve Group and Supra Inguinal Fascia Iliaca BLOCK for Analgesia and Ease of Positioning During Neuraxial Anesthesia in Hip Fracture Patients

Not Applicable
Completed
Conditions
Spinal Anesthesia
Hip Fractures
Interventions
Procedure: pericapsular nerve group block
Procedure: suprainguinal fascia iliaca block
Registration Number
NCT05987254
Lead Sponsor
Al-Azhar University
Brief Summary

Severe pain associated with fractured hip often results in difficulty during positioning for spinal anesthesia (SA). Among many regional analgesic techniques, the fascia iliaca compartment block (FICB) is popular among anesthesiologists to provide immediate as well as postoperative analgesia in hip fractures. Recently, the pericapsular nerve group (PENG) block has been proposed to provide effective analgesia in hip fracture patients. However, comparative studies between PENG and FICB are lacking.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • 40 years and above with hip fracture with persistent pain and scheduled for surgery under spinal anesthesia (SA)
Exclusion Criteria
  • any contraindications to SA or peripheral nerve blocks, history of ischaemic heart disease, patients on opioids for chronic pain and patients with significant cognitive impairment. Patients who had no pain while sitting by themselves (resting pain less than 4 on NRS) for SA without any support were also excluded.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PENG grouppericapsular nerve group blockreceived ultrasound guided pericapsular nerve group block
FICB groupsuprainguinal fascia iliaca blockreceived ultrasound guided suprainguinal fascia iliaca block
Primary Outcome Measures
NameTimeMethod
The ease of spinal positioning (EOSP)Thirty minutes after the blocks

The ease of spinal positioning (EOSP) was assessed on the scale of 0-3 (0 = unable to position, 1 = patient had abnormal posturing due to pain and required support for positioning, 2 = mild discomfort but does not require support for positioning, 3 = optimal condition where the patient was able to position himself without pain)

NRS30 minute postoperative

In a Numerical Rating Scale (NRS), patients are asked to circle the number between 0 and 10, that fits best to their pain intensity. Zero usually represents 'no pain at all' whereas the upper limit represents 'the worst pain ever possible'.

Secondary Outcome Measures
NameTimeMethod
amount of tramadol used24 hours postoperatively

number of rescue doses of tramadol will be recorded

Trial Locations

Locations (3)

Haney Baumey

🇪🇬

Banhā, Egypt

Facualty of Pharmacy, Al Azhar University

🇪🇬

Cairo, Egypt

Neveen Kohaf

🇪🇬

Tanta, Egypt

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