FRONT Block for Quality of Recovery After Total Hip Arthroplasty
Condition(s) studied
Investigational drug(s) / intervention(s)
FRONT Block (Femoral Rami and Obturator Nerve Trunk Block): Ultrasound-guided unilateral FRONT block targeting the femoral rami and obturator nerve trunk will be performed
Standard Multimodal Analgesia: Standardized postoperative multimodal analgesia including intravenous paracetamol, nonsteroidal anti-inflammatory drugs, and rescue opioid analgesia as required.
Study summary
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.
Eligibility
Primary outcome measure(s)
- Postoperative Quality of Recovery (QoR-15 Score) — 24 hours after surgery
Postoperative quality of recovery will be assessed using the validated Quality of Recovery-15 (QoR-15) questionnaire. The total score ranges from 0 to 150, with higher scores indicating better recovery.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Betul Kozanhan | Konya | Turkey (Türkiye) | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07458360 on ClinicalTrials.gov ↗ ← All trials in Turkey