Actively Recruiting
FRONT Block for Quality of Recovery After Total Hip Arthroplasty
Led by Konya Meram State Hospital · Updated on 2026-04-28
80
Participants Needed
1
Research Sites
10 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
FRONT Block for Quality of Recovery After Total Hip Arthroplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age �3A 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 will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Betul Kozanhan
Konya, Turkey (Türkiye), 42005
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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