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临床试验/NCT02175576
NCT02175576终止不适用

Randomized Controlled Clinical Outcomes of the Vanguard XP Bicruciate Knee System

Zimmer Biomet4 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2014年10月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
Zimmer Biomet
入组人数
50
试验地点
4
主要终点
Number of Knees Reported as "Feels Normal" on a Single Assessment Numeric Evaluation (SANE)

研究概览

简要总结

Randomized Controlled Study to determine if preservation of ligaments provides increased functional ability post-operatively in comparison to traditional TKA which sacrifices soft tissue.

详细描述

Randomized Controlled Study to compare clinical and patient reported outcomes of the Vanguard XP Bicruciate Total Knee System to the Vanguard CR Knee System through 10 years of follow-up.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • cemented application of components
  • bilateral subjects randomized by knee
  • patients with pre-existing contralateral knee surgery
  • painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, or traumatic arthritis where one or more compartments are involved
  • correction of varus, valgus, or posttraumatic deformity
  • sufficient soft tissue surrounding the knee, including the Anterior Cruciate Ligament

排除标准

  • cementless application of components
  • BMI greater than or equal to 40
  • use of Anterior Stabilized Bearings
  • patients with severe pre-operative varus or valgus deformity greater than or equal to 15 degrees
  • correction or revision of previous joint replacement procedure on index knee
  • infection
  • osteomyelitis
  • Relative exclusion criteria:
  • uncooperative patient or patient with neurological disorders who is incapable of following directions
  • osteoporosis
  • metabolic disorders which may impair bone formation
  • osteomalacia
  • distant foci of infections which may spread to the implant site
  • rapid joint destruction, marked bone loss, or bone resorption apparent on roentgenogram
  • vascular insufficiency, muscular atrophy, neuromuscular disease
  • incomplete or deficient soft tissue surrounding the knee, including the anterior cruciate ligament

结局指标

主要结局

Number of Knees Reported as "Feels Normal" on a Single Assessment Numeric Evaluation (SANE)

时间窗: 12 Months

Participants answered a Single Assessment Numeric Evaluation (SANE) which asked how they rated their knee function. A score of 100 indicates normal and anything below 100 indicates a percentage of normal function.

次要结局

  • Number of Knees Reported as "Feels at Least 80% of Normal" on a Single Assessment Numeric Evaluation (SANE)(12 Months)
  • Revisions/Removals(3 years)
  • Modified Knee Society Score(12 months)
  • Number of Knees With Which Participants Reported Being "Happy" or "Very Happy"(12 Months)

研究者

发起方
Zimmer Biomet
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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