FRONT Block for Quality of Recovery After Total Hip Arthroplasty
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKonya Meram State Hospital
About this trial
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 criteria
Qualifiers
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
Disqualifiers
Refusal to participate
Contraindication to spinal anesthesia or regional block
Allergy to study medications
Chronic opioid use (daily use for more than 3 months)
Trial design
Treatments tested in this trial
- FRONT Block (Femoral Rami and Obturator Nerve Trunk Block)
- Standard Multimodal Analgesia
Treatment groups
80 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov