About this trial
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.
Eligibility criteria
Qualifiers
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
Disqualifiers
Refusal to participate
Contraindications to spinal anesthesia
Contraindications to regional anesthesia
Allergy to local anesthetics or study medications
Trial design
Treatments tested in this trial
- Quadro-Iliac Plane Block
- Suprainguinal Fascia Iliaca Block
- Standard Multimodal Analgesia