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临床试验/NCT06858358
NCT06858358招募中不适用

Comparison of Robotic-Assisted Medial Congruent and Conventional Medial Pivot Total Knee Arthroplasty: a Prospective, Multicenter Analysis

George Emil Palade University of Medicine, Pharmacy, Sciences and Technology of Targu Mures4 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2025年2月24日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
300
试验地点
4
主要终点
Polyethylene insert thickness

研究概览

简要总结

This multicenter, prospective cohort study will evaluate whether Robotic-Assisted total knee arthroplasty (RATKA) with a Medial Congruent implant is a successful method to improve implant alignment, insert thickness accuracy, and patient satisfaction, compared to a conventional TKA (cTKA) Medial Pivot technique. It aims to assess and compare clinical and functional outcomes in patients with severe knee osteoarthritis at 3, 6, and 12 months.

详细描述

This prospective, non-randomized, multicenter trial evaluates robotic-assisted (ROSA® Robotic Platform with Zimmer Biomet Persona® Medial Congruent) versus conventional (MicroPort Evolution® Medial-Pivot) total knee arthroplasty (TKA) in approximately 300 adults with severe osteoarthritis. By comparing robotic precision with a well-established Medial-Pivot design, this investigation aims to clarify whether robotic-assisted TKA confers superior implant positioning, reduced alignment outliers, and enhanced patient-reported outcomes (PROMS). The primary outcome measures include insert thickness, alignment accuracy (outliers defined as >2° from the mechanical axis on full-leg radiographs), and patient satisfaction at 6 and 12 months. Two surgeons will perform both techniques, and one surgeon will perform only the conventional procedure. The 18-month study is conducted under local Institutional Review Board approvals (Medlife, Medicover, SCJU Cluj Napoca, Monza Bucuresti) and complies with GDPR. Results are intended for publication in a high-impact orthopedic journal. No external funding is provided.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with severe osteoarthritis (greater than III Ahlback)

排除标准

  • Patients who refuse participation in the study Low-grade osteoarthritis

结局指标

主要结局

Polyethylene insert thickness

时间窗: Perioperative/ Periprocedural

Insert Thickness: Measured and analyzed in millimeters

Mechanical axis outliers

时间窗: Perioperative/ Periprocedural

Outliers: Defined as more than 2.0 degrees from mechanical alignment, measured on full-leg X-ray

次要结局

  • International knee documentation committe (IKDC) subjective score(3, 6, and 12 months post-operative)
  • Forgotten joint score-12 (FJS-12)(3, 6, and 12 months post-operative)

研究者

发起方
George Emil Palade University of Medicine, Pharmacy, Sciences and Technology of Targu Mures
申办方类型
Other
责任方
Principal Investigator
主要研究者

Marian Andrei Melinte

Principal investigator

George Emil Palade University of Medicine, Pharmacy, Sciences and Technology of Targu Mures

研究点 (4)

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