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OpenTrials
Completed

NCT Number: NCT06838156

Comparison of Analgesic Efficacy of Quadratus Lumborum Type 3 and Suprainguinal Fascia Iliaca Compartment Block in Total Hip Arthroplasty Surgery

Total Hip Arthroplasty (THA) is a complex surgical procedure frequently performed to treat degenerative conditions in the hip joint. As people's life expectancy increases, the need for hip arthroplasty increases. İnvestigetors aimed to compare the analgesic properties of SIFI and QLB blocks.

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Key information

Conditions

Opioid Consumption Neurologic Manifestations Pain Pain Postoperative Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Postoperative Complications Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Başakşehir Çam Ve Sakura City Hospital

Başakşehir, Istanbul, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Elective patients scheduled for hip arthroplasty surgery
  • Patient willingness to participate in the study
  • Patients over 18 years age of, ASA I-II-III,

Exclusion criteria

  • Patients not wanting to participate in the study
  • Patients who do not want regional anesthesia technique
  • Allergic or coagulated patients
  • Patients with liver, kidney, lung, heart failure and septic patients
  • Neurological disorder, history of convulsions
  • ASA IV patients

Treatment and study plan

Bupivacain

Drug

Suprainguinal Fascia Iliaca Compartment block was performed with a linear probe placed over the inguinal ligament using a portable ultrasound device. After visualization of the femoral nerve, 30 ml of 0.25% bupivacaine was injected into the fascia iliaca overlying the iliopsoas muscle using an appropriate needle.

Other names: SIFI

Primary outcomes

  1. Effect on pain score

    Time frame: At 1,2,4, 6, 12 and 24 hours after surgery

    Postoperative 24-hour Visual Analog Scale was measured. ( 0=best 10=worst)

Secondary outcomes

  1. Opioid Consumption

    Time frame: At 1,2,4, 6, 12 and 24 hours after surgery

    Intravenous patient-controlled analgesia (PCA) with tramadol was administered to both groups in the postoperative period.

Sponsors and collaborators

Lead sponsor

Başakşehir Çam & Sakura City Hospital

Other Gov

Registry information

Official study title

Comparison of Analgesic Efficacy of Quadratus Lumborum Type 3 and Suprainguinal Fascia Iliaca Compartment Block in Total Hip Arthroplasty Surgery: A Randomized Controlled Trial

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Feb 20, 2025
Registry last updated
Feb 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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