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FRONT Block for Quality of Recovery After Total Hip Arthroplasty

RECRUITINGN/ASponsored by Konya Meram State Hospital
Actively Recruiting
PhaseN/A
SponsorKonya Meram State Hospital
Started2026-04-25
Est. completion2026-06-05
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →

NCT07458360

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

Age: 18 Years+Healthy volunteers accepted
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

Conditions4

ArthritisOsteoarthritis of the HipPostoperative PainQuality of Recovery

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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