Actively Recruiting
Comparison of Analgesic Efficacy of Suprainguinal Fascia Iliaca and Quadro-iliac Blocks in Hip Fracture Surgery
Led by Hitit University · Updated on 2026-04-23
70
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Hip fractures are common in the elderly and are associated with significant morbidity and mortality. Effective early analgesia is crucial for facilitating mobilization, reducing pulmonary complications, and improving overall outcomes. Although opioids are traditionally used for postoperative pain management, their adverse effects have led to increased interest in multimodal analgesia, particularly peripheral nerve blocks. The suprainguinal fascia iliaca block (SIFI) is a modified technique that allows wider spread of local anesthetic, providing more effective blockade of the femoral, obturator, and lateral femoral cutaneous nerves. The quadro-iliac plane block (QIPB), a recently described interfascial block, is performed at the level of the anterior superior iliac spine and may also affect branches of the lumbar and sacral plexus. While both techniques have been shown to provide effective analgesia and reduce opioid consumption, there is no study directly comparing them. Therefore, this study aims to compare the postoperative analgesic efficacy of SIFI and QIPB in patients undergoing hip fracture surgery.
CONDITIONS
Official Title
Comparison of Analgesic Efficacy of Suprainguinal Fascia Iliaca and Quadro-iliac Blocks in Hip Fracture Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years and older
- ASA physical status I-III
- Hemodynamically stable patients
- Scheduled for surgical treatment of hip fracture
- Body mass index (BMI) 35 kg/m8
- Provided written informed consent
You will not qualify if you...
- Refusal to participate
- ASA physical status IV-V
- Hemodynamically unstable patients
- Surgery not completed as planned
- Infection at the block site
- History of allergy to local anesthetics or tramadol
- Presence of neuromuscular or peripheral nerve diseases
- Chronic pain conditions
- Coagulopathy or ongoing anticoagulant therapy
- High-dose opioid use within the last 3 days
- Severe hepatic or renal insufficiency
- Diabetes mellitus
- Pregnancy or breastfeeding
- Numeric rating scale (NRS) score 7 for four consecutive hours despite multimodal analgesia
- Inability to understand or use assessment tools (e.g., NRS, QoR-15)
- Inability to communicate in Turkish
- Inability to use patient-controlled analgesia (PCA) device due to technical reasons
AI-Screening
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Trial Site Locations
Total: 1 location
1
Hitit university
Çorum, Turkey (Türkiye), 19100
Actively Recruiting
Research Team
M
MUHAMMED ATICI
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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