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Lumbar Erector Spinae Plane Block and Fascia Iliaca Compartment Block After Total Hip Arthroplasty

Comparative Study Between Ultrasound-Guided Lumbar Erector Spinae Plane Block and Fascia Iliaca Compartment Block for Postoperative Analgesia After Total Hip Arthroplasty

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05905510
Enrollment
75
Registered
2023-06-15
Start date
2023-06-15
Completion date
2023-12-01
Last updated
2023-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesia

Brief summary

Compare the analgesic efficacy of ultrasound-guided lumbar erector spinae plane block (L-ESPB) versus fascia iliaca compartment block (FICB) in patients scheduled for total hip arthroplasty.

Detailed description

Ultrasound-guided erector spinae plane (ESP) block is a recent regional anesthetic technique. It was first described by Forero et al. in 2016 for acute and chronic thoracic pain management. Local anesthetic (LA) is injected between the erector spinae muscle and the vertebra's transverse process, leading to the spread of LA cephalad, caudally, and through the paravertebral space.

Interventions

The fourth lumbar vertebral level will be determined using the conventional method (the imaginary line between two crista iliacas). The convex transducer will be placed at the mid-vertebral line in the sagittal plane. The transducer will be shifted from the midline, 3.5-4 cm laterally, to the side of the surgery to visualize the erector spinae muscle and transverse process. Using the out-of-plane technique, a 22G/80-mm block needle will be advanced until it reached the transverse process. 0.5-1 ml of the prepared local anesthesia solution (30 ml bupivacaine 0.25%) will be administered, leading to hydro dissection to confirm the correct location. The needle will be repositioned by pulling back a few millimeters if resistance occurred when administering local anesthesia. All local anesthesia will be administered to this location between the transverse process and the erector spinae muscle

The transducer will be placed laterally to the femoral nerve. It then rotated 90 degrees to the sagittal plane, under ultrasound guidance, a regional block needle (22 G, 80 mm) will be introduced in the cranial direction. Once good needle alignment with the ultrasound beam is achieved, the needle will be inserted deep into the tissues until an optimal position of the needle tip is obtained. Needle location will be additionally verified by injecting 0.5-1 ml of the prepared local anesthesia solution and observing the solution spread within the tissues. Once the correct position of the needle tip is confirmed, the local anesthetic will be deposited under the iliac fascia to force its flow towards the lumbar plexus. 30 ml of bupivacaine 0.25% solution will be used for the block. local anesthesia will be administered as 5 mL boluses with a 20 second interval.

DRUGspinal anesthesia plane block

Patients will receive spinal anesthesia alone

Sponsors

Tanta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Patients aged 30-75 years from both sexes. 2. ASA I-III scheduled for unilateral hip surgery under spinal anesthesia.

Exclusion criteria

1. Patients' refusal. 2. Patients who were unable to co-operate with researchers. 3. History of allergy to local anesthetics. 4. Local infection at the site of the block. 5. Patients with bleeding and coagulation disorders. 6. Patients with renal, hepatic, cardiac decompensation, or spine deformities. 7. Patients receiving opioids for chronic analgesic therapy 8. Body mass index \> 35 kg/m2

Design outcomes

Primary

MeasureTime frameDescription
Assessment of postoperative painUP to 24 hour postoperativelyAssessment of postoperative pain using the Numeric rating scale (NRS), NRS is a valid and simple approach to pain assessment (0= no pain and 10= worst possible pain)

Secondary

MeasureTime frameDescription
Time required for the first rescue analgesia.Up to 24 hours postoperativelyMorphine sulfate 0.03 mg/kg will be administered intravenous as a rescue analgesic if Numeric rating scale is ≥ 4
The total postoperative rescue analgesicfirst 24 hours postoperativelyThe total amount of morphine consumption
Adverse effectsUp to 24 hours postoperativelyAny complications or undesirable side effects will be observed and treated.

Countries

Egypt

Contacts

Primary ContactAhmed Ahmed Zahran, MBBCH
ahmad162088@med.tanta.edu.eg+20 101 997 6377

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026