Comparison of Three Analgesic Strategies for Hip Fracture Surgery
Starting soon · Not applicable
Conditions studied: Hip Fracture
In brief
Hip fracture surgery is associated with significant postoperative pain and increased opioid requirements. Regional anesthesia techniques may improve analgesia and reduce opioid consumption. This prospective, randomized, double-blind, controlled trial aims to compare the postoperative analgesic efficacy of Quadro-Iliac Plane Block (QIPB), Suprainguinal Fascia Iliaca Block (SIFIB), and standard analgesia in patients undergoing hip fracture surgery under spinal anesthesia. The primary outcome is cumulative tramadol consumption during the first 24 postoperative hours. Secondary outcome measures include postoperative pain intensity, rescue analgesic requirement, incidence of postoperative nausea and vomiting, Quality of Recovery-15 (QoR-15) score, and patient satisfaction score.
Key facts
- Study ID
- NCT07676734
- Run by
- Başakşehir Çam & Sakura City Hospital
- People needed
- 90
- Starts
- 2026-07-15
- Expected to finish
- 2027-02-01
- Last updated by the study team
- 2026-06-30
Who can join
Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult patients aged 18 years or older
- Patients scheduled for hip fracture surgery under spinal anesthesia
- American Society of Anesthesiologists (ASA) physical status I-III
- Provision of written informed consent
You may not qualify if…
- Refusal to participate
- Contraindications to spinal anesthesia
- Contraindications to regional anesthesia
- Allergy to local anesthetics or study medications
- Infection at the injection site
- Coagulopathy or anticoagulant therapy precluding regional block
- Cognitive impairment preventing pain assessment
- Chronic opioid use
- Revision surgery
Where it is running
- Başakşehir Çam and Sakura City Hospital — Istanbul, Istanbul, Turkey (Türkiye)
Full record on ClinicalTrials.gov
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