Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07452120

Comparison of Deep Iliacus Plane Block and Suprainguinal Fascia Iliaca Block for Postoperative Pain Control in Hip Surgery Patients

Led by Sivas Numune Hospital · Updated on 2026-04-02

70

Participants Needed

2

Research Sites

4 weeks

Total Duration

On this page

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older
  • ASA physical status I-III
  • Scheduled for elective primary total hip arthroplasty under spinal anesthesia
  • Able to understand study procedures and provide informed consent
Not Eligible

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

Trial Site Locations

Total: 2 locations

1

Sivas Numune Hospital

Sivas, Sivas, Turkey (Türkiye), 58050

Not Yet Recruiting

2

Sivas Numune Hospital

Sivas, Turkey (Türkiye)

Actively Recruiting

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Research Team

F

Fatih Balcı, MD

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

Ultrasound-guided Deep Iliacus Plane Block (DIPB): Cadaveric Evaluation and Pilot Retrospective Evaluation of Another Novel Fascial Plane Block for Hip Analgesia.

Serkan Tulgar, Bahadır Çiftçi, Bediha Koyuncu...

https://pubmed.ncbi.nlm.nih.gov/41498358

Efficacy of Different Volumes of 0.2% Ropivacaine in Suprainguinal Fascia Iliaca Compartment Block for Multimodal Analgesia in Lower Limb Surgery.

Jessica Sekhon, Richa Jain, Kamya Bansal...

https://pubmed.ncbi.nlm.nih.gov/37954742

Implementation of the Obturator Nerve Block into a Supra-Inguinal Fascia Iliaca Compartment Block Based Analgesia Protocol for Hip Arthroscopy: Retrospective Pre-Post Study.

Seounghun Lee, Jung-Mo Hwang, Sangmin Lee...

https://pubmed.ncbi.nlm.nih.gov/32230895

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.

Lalisa Saeaeh, Theerawat Chalacheewa, Chatchawat Lerdwimonsak...

https://pubmed.ncbi.nlm.nih.gov/41023795