QIPB vs SI-FICB for Postoperative Analgesia After Total Hip Arthroplasty

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorDokuz Eylul University

About this trial

Total hip arthroplasty (THA) causes moderate-to-severe postoperative pain. The PROSPECT guideline recommends the supra-inguinal fascia iliaca compartment block (SI-FICB) for THA, whereas evidence for newer quadratus-lumborum-family blocks is limited. The quadro-iliac plane block (QIPB) is a recently described fascial plane block, and no study has compared QIPB with SI-FICB head-to-head in any surgical context. In this prospective, double-blind, patients undergoing elective THA who receive one of the two routinely used preoperative blocks (SI-FICB or QIPB, chosen by the attending anesthesiologist as part of routine care) are systematically observed and compared. The primary objective is to assess whether the postoperative analgesic efficacy of QIPB is non-inferior to SI-FICB, using the resting NRS pain score at 6 hours postoperatively as the primary endpoint (non-inferiority margin Δ = 1.3).

Eligibility criteria

Qualifiers

Adults aged 18-75 years

Scheduled for elective primary total hip arthroplasty

ASA physical status I-III

Able to understand and communicate in Turkish and complete assessment scales

Disqualifiers

Known allergy/contraindication to any local anesthetic, including bupivacaine

Coagulopathy or anticoagulant/antiplatelet therapy contraindicating block (per ASRA 2022)

Active infection or skin breakdown at the block site

Chronic opioid use (≥3 months daily) or history of opioid dependence

Trial design

Treatments tested in this trial

  • Supra-Inguinal Fascia Iliaca Compartment Block
  • Quadro-Iliac Plane Block

Treatment groups

84 Participants
are divided into 2 treatment groups

Sponsors and collaborators