MedPath

Ultrasound-Guided Popliteal Plexus Block Versus Fascia Iliaca Block After Total Knee Arthroplasty

Not Applicable
Completed
Conditions
Popliteal Plexus Block
Fascia Iliaca Block
Total Knee Arthroplasty
Interventions
Device: Ultrasound-Guided Popliteal Plexus Block
Device: Ultrasound-Guided Fascia Iliaca block
Registration Number
NCT05390450
Lead Sponsor
Tanta University
Brief Summary

This study aims to investigate the effect of the Popliteal Plexus Block versus Fascia Iliaca Block on postoperative pain after total knee arthroplasty.

Detailed Description

The Popliteal Plexus entwines the popliteal artery and vein contiguous to the adductor hiatus in the popliteal fossa and innervates the posterior capsule as well as intraarticular genicular structures. It was recently confirmed in a cadaver study that injection of 10 mL of dye into the distal end of the adductor canal spreads via the adductor hiatus to the popliteal fossa and stains the Popliteal Plexus.

Recently, fascia iliaca block was proposed as a popular analgesic technique which involves local infiltration anesthesia under the fascia of the iliacus muscle. The method depends on the local anesthetics spread beneath the fascia to block the peripheral nerve. It has been proposed to avoid the complications by anesthetizing the femoral nerve remotely from major neurovascular structures and achieve adequate analgesia.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Age 40 - 75 years.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) score I-II.
  • Scheduled for unilateral, primary TKA under spinal anesthesia.
Read More
Exclusion Criteria
  • Coagulopathy.
  • Diabetes.
  • Obesity.
  • Heart failure.
  • kidney failure.
  • Liver failure.
  • Reduced sensation on the lower limb.
  • Daily intake of opioids.
  • Contraindication to any drug used in the study.
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Ultrasound-Guided Popliteal Plexus BlockUltrasound-Guided Popliteal Plexus BlockPatients in this group will receive Popliteal plexus block.
Ultrasound-Guided Fascia Iliaca blockUltrasound-Guided Fascia Iliaca blockPatients in this group will receive Fascia Iliaca block.
Primary Outcome Measures
NameTimeMethod
Total intravenous (IV) morphine consumption24 hours postoperatively.

Total intravenous (IV) morphine consumption during the first postoperative 24 hours, postoperatively.

Secondary Outcome Measures
NameTimeMethod
First analgesic request24 hours postoperatively

Time to first analgesic request after surgery in the form of intravenous morphine in a dose (0.05 mg/kg).

Pain level score24 hours postoperatively

Pain levels using the numerical rating scale (NRS) of pain intensity (0 = no pain) to (10 = intolerable pain), pain relief is defined as a NRS of 3 or lower. If the score is \>3, the patient will need analgesia in the form of morphine 0.05 mg/kg till it decreases to ≤3. NRS will be assessed and recorded on arrival to Post-Anesthesia Care Unit , 1, 2, 4, 8, 12 and 24 hours postoperatively at rest and on movement (knee flexion) during the first postoperative 24 hours.

Patient's satisfaction level24 hours postoperatively

Degree of patient satisfaction will be assessed on a 5-point scale; (1= highly satisfied, 2 = satisfied, 3 = neither satisfied nor unsatisfied, 4 = not satisfied, 5 = highly not satisfied)

Rehabilitation24 hours postoperatively

Rehabilitation (time to ability to sit, time to ability to stand, time to ability to walk, Time to ability to do exercise) will be recorded.

Trial Locations

Locations (1)

Tanta University Hospitals

🇪🇬

Tanta, Elgharbia, Egypt

© Copyright 2025. All Rights Reserved by MedPath