FRONT Block for Quality of Recovery After Total Hip Arthroplasty
Recruiting · NCT07458360 · Interventional (participants receive a specific treatment) · Lead sponsor: Konya Meram State Hospital
View the official record on ClinicalTrials.gov →Interventions studied
FRONT Block (Femoral Rami and Obturator Nerve Trunk Block)Standard Multimodal Analgesia
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.
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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
Where it is running
1 location listed.
- Betul Kozanhan - Konya, Turkey (Türkiye)