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

Not Applicable

Completed

• Conditions: Opioid Consumption; Pain Postoperative
• Interventions: Drug: Bupivacain

• Registration Number: NCT06838156
• Lead Sponsor: Başakşehir Çam & Sakura City Hospital

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study Start: 2023-02-15
• Primary Completion: 2023-06-15
• Study Completion: 2023-08-01
• Status Verified: 2025-02
• Study First Submitted: 2025-02-09
• Study First Submitted QC: 2025-02-18
• Last Update Submitted: 2025-02-18
• Study First Posted: 2025-02-20
• Last Update Posted: 2025-02-20

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

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

Exclusion Criteria

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
SIFI Group	Bupivacain	Group of 30 patients who underwent SIFI block
QLB Type 3	Bupivacain	Group of 30 patients who underwent QLB block

Primary Outcome Measures

Name	Time	Method
Effect on pain score	At 1,2,4, 6, 12 and 24 hours after surgery	Postoperative 24-hour Visual Analog Scale was measured. ( 0=best 10=worst)

Secondary Outcome Measures

Name	Time	Method
Opioid Consumption	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.

Trial Locations

Locations (1)

Başakşehir Çam Ve Sakura City Hospital; 🇹🇷 Başakşehi̇r, İ̇stanbul, Turkey