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RecruitingNot ApplicableNCT07458360

FRONT Block for Quality of Recovery After Total Hip Arthroplasty

Effect of Femoral Rami and Obturator Nerve Trunk (FRONT) Block on Postoperative Quality of Recovery After Total Hip Arthroplasty: A Prospective Randomized Controlled Trial

Sponsor

Konya Meram State Hospital

Enrollment

80 participants

Start Date

Apr 25, 2026

Study Type

INTERVENTIONAL

Conditions

Quality of recoveryPostoperative PainOsteoarthritis of the hip

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

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called FRONT Block (Femoral Rami and Obturator Nerve Trunk Block) and a procedure called Standard Multimodal Analgesia for people with osteoarthritis of the hip, postoperative pain, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREFRONT Block (Femoral Rami and Obturator Nerve Trunk Block)

Ultrasound-guided unilateral FRONT block targeting the femoral rami and obturator nerve trunk will be performed

PROCEDUREStandard Multimodal Analgesia

Standardized postoperative multimodal analgesia including intravenous paracetamol, nonsteroidal anti-inflammatory drugs, and rescue opioid analgesia as required.

Locations(1)

Betul Kozanhan

Konya, Turkey (Türkiye)

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NCT07458360

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