Comparison of Three Analgesic Strategies for Hip Fracture Surgery

ConditionHip Fracture
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorBaşakşehir Çam & Sakura City Hospital

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

Treatment groups

90 Participants
are divided into 3 treatment groups