FRONT Block for Quality of Recovery After Total Hip Arthroplasty

Recruiting now · Not applicable

Conditions studied: Osteoarthritis of the Hip, Postoperative Pain, Quality of Recovery

In brief

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.

Key facts

Study ID

NCT07458360

Run by

Konya Meram State Hospital

People needed

80

Starts

2026-04-25

Expected to finish

2026-08-05

Last updated by the study team

2026-07-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Betul Kozanhan — Konya, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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