Clinical Trial

High-Strength Suture vs. Traditional Tension Band for Patellar Fractures

Recruiting
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Record status
This record was last updated November 25, 2025 (before its estimated February 28, 2026 completion). Its status may not reflect the trial's current state.
Summary
This prospective cohort study aims to evaluate the clinical efficacy of high-strength suture modified tension band fixation in treating patellar fractures and compare it with traditional screw-cable tension band fixation. Adult patients (18-55 years) with AO/OTA 34-C1 or 34-C2 patellar fractures will be enrolled and followed for 12 months. Primary outcomes include Lysholm knee function score, knee range of motion (ROM), and visual analog scale (VAS) pain score at 12 months post-surgery. Secondary outcomes include fracture healing time, radiographic alignment quality, complication rates, reoperation rates, implant removal rates, SF-36 health survey scores, and patient satisfaction. No additional biological samples will be collected; data will focus on clinical, radiographic, and follow-up information.
Trial Details
NCT Number NCT07248982
Lead Sponsor Fuzhou University Affiliated Provincial Hospital
Conditions Patella Fracture
Enrollment 50 participants
Start Date 2024-02-01
Primary Completion 2026-02-28 (estimated)
Study Completion 2026-06-30 (estimated)
Updated on ClinicalTrials.gov 2025-11-25