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FRONT Block for Quality of Recovery After Total Hip Arthroplasty

RecruitingNAAges 18 Years - anyAllKonya Meram State Hospital
NCT07458360 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This prospective randomized controlled trial evaluates the effect of ultrasound-guided unilateral Femoral Rami and Obturator Nerve Trunk (FRONT) block on postoperative quality of recovery in patients undergoing elective total hip arthroplasty.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Age ≥ 18 years * Scheduled for total hip arthroplasty under spinal anesthesia * American Society of Anesthesiologists (ASA) physical status I-III * Ability to understand and complete the QoR-15 questionnaire * Provided written informed consent Exclusion Criteria: * Refusal to participate * Contraindication to spinal anesthesia or regional block * Allergy to study medications * Chronic opioid use (daily use for more than 3 months) * Neurological or neuromuscular disorders affecting the lower extremities * Infection at the injection site * Coagulation disorders * Cognitive impairment prevents questionnaire completion
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What it tests

  • FRONT Block (Femoral Rami and Obturator Nerve Trunk Block)
  • Standard Multimodal Analgesia
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Where

1 site
Betul Kozanhan
Konya, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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