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FRONT Block for Quality of Recovery After Total Hip Arthroplasty

NCT07458360 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2026-07-28

No results posted yet for this study

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.

Conditions

  • Osteoarthritis of the Hip
  • Postoperative Pain
  • Quality of Recovery

Interventions

PROCEDURE

FRONT Block (Femoral Rami and Obturator Nerve Trunk Block)

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

PROCEDURE

Standard Multimodal Analgesia

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

Sponsors & Collaborators

  • Konya Meram State Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-04-25
Primary Completion
2026-08-05
Completion
2026-08-05

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07458360 on ClinicalTrials.gov