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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: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Turkey
Betul Kozanhan
RECRUITING
Konya
Time Frame
Start Date: 2026-04-25
Estimated Completion Date: 2026-07-05
Participants
Target number of participants: 80
Treatments
Experimental: FRONT Block Group
Participants in this group will receive an ultrasound-guided unilateral Femoral Rami and Obturator Nerve Trunk (FRONT) block in addition to standardized multimodal postoperative analgesia.
Active_comparator: Control Group
Participants in this group will receive standardized multimodal postoperative analgesia without FRONT block.
Sponsors
Leads: Konya Meram State Hospital

This content was sourced from clinicaltrials.gov