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Not Yet RecruitingNCT07458360

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

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Konya Meram State Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed description

Total hip arthroplasty (THA) is associated with significant postoperative pain that may impair early recovery. The Femoral Rami and Obturator Nerve Trunk (FRONT) block is a regional anesthesia technique targeting sensory innervation of the anterior hip capsule and may improve postoperative recovery while preserving motor function. This prospective randomized controlled trial aims to evaluate whether the addition of ultrasound-guided unilateral FRONT block to standard multimodal analgesia improves postoperative quality of recovery in patients undergoing THA.

Conditions

Interventions

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

Timeline

Start date
2026-03-10
Primary completion
2026-06-05
Completion
2026-07-05
First posted
2026-03-09
Last updated
2026-03-09

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07458360. Inclusion in this directory is not an endorsement.