Comparing Deep Iliacus Plane Block and Suprainguinal Fascia Iliaca Block for Pain Relief After Hip Replacement Surgery
Led by Sivas Numune Hospital · Updated on 2026-04-02
70
Participants Needed
2
Research Sites
4 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are comparing two types of nerve block techniques, the Deep Iliacus Plane Block DIPB and the Suprainguinal Fascia Iliaca Block SIFIB, to manage pain after primary total hip arthroplasty surgery. The goal is to find out which method provides better pain relief with fewer side effects like motor weakness. This clinical trial is randomized, double-blind, and controlled, involving patients under spinal anesthesia undergoing hip replacement.
Seventy patients will be randomly assigned to receive either DIPB or SIFIB at the end of their surgery. Both procedures involve ultrasound-guided injections of 0.25% bupivacaine 30-40 mL adjusted by weight for postoperative pain control. The SIFIB targets mainly the femoral and lateral femoral cutaneous nerves but may miss deeper joint nerves, while DIPB aims to cover both superficial and deep nerves with potentially less motor impairment.
Participants will be monitored for 48 hours after surgery, with pain levels measured at rest and during movement at specific times up to 48 hours. Opioid use, motor block severity using the modified Bromage scale, and any complications related to the blocks will also be recorded. This study assesses pain intensity, opioid consumption, motor block, and other outcomes to determine the best approach for safe and effective pain management after hip arthroplasty.
CONDITIONS
Brief Title
DIPB vs. SIFIB for Postoperative Analgesia After Hip Surgery
Research Team
F
Fatih Balcı, MD
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Scheduled for elective primary total hip arthroplasty under spinal anesthesia
Able to understand study procedures and provide informed consent
You will not qualify if you...
Blood clotting disorders or use of blood thinners that prevent regional anesthesia
Infection at the site of nerve block application
Hemodynamic instability
Known allergy to local anesthetics
Significant neurological or motor deficits in lower limbs
Cognitive impairment preventing pain assessment
Refusal or inability to provide informed consent
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Surgery and Immediate Post-operative Care
Duration - Day of surgery
Participants undergo elective primary total hip arthroplasty under spinal anesthesia and receive the assigned nerve block (either Deep Iliacus Plane Block or Suprainguinal Fascia Iliaca Block) at the end of surgery for postoperative pain control.
1 visit (in-person)
Post-operative Follow-up
Duration - 48 hours postoperatively
Participants are monitored for postoperative pain, opioid consumption, motor block, and adverse events up to 48 hours after surgery.
Multiple assessments during hospital stay up to 48 hours
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Published Research Related To This Trial
Implementation of the Obturator Nerve Block into a Supra-Inguinal Fascia Iliaca Compartment Block Based Analgesia Protocol for Hip Arthroscopy: Retrospective Pre-Post Study.
Ultrasound-guided Deep Iliacus Plane Block (DIPB): Cadaveric Evaluation and Pilot Retrospective Evaluation of Another Novel Fascial Plane Block for Hip Analgesia.
Comparison between combined suprainguinal fascia iliaca compartment block with intra-articular bupivacaine and suprainguinal fascia iliaca compartment block in total hip arthroplasty: randomized double blinded controlled trial.