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临床试验/NCT02482493
NCT02482493暂停不适用

A Prospective Randomised Control Trial to Compare Clinical and Radiological Outcomes of the Press-Fit Condylar All-Polyethylene Tibial Component With Metal-Backed Tibial Component Implant, in Patients Aged 75 Years or Over

Maidstone & Tunbridge Wells NHS Trust2 个研究点 分布在 1 个国家目标入组 88 人开始时间: 2017年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
暂停
发起方
入组人数
88
试验地点
2
主要终点
American Knee Society Score

研究概览

简要总结

Total knee arthroplasty (TKA) is one of the most commonly performed orthopaedic procedures. Approximately 84,000 knee replacement procedures were recorded in the UK in 2012. The main goal of TKA is to relieve the disabling pain of arthritic disease.

Patient satisfaction following TKA is related to quick recovery and return to daily activities. This can be dependent on the design of the implant used in the knee. Improvements in implant design and surgical technique mean many modern designs offer implant survival rates beyond 10 - 15 years.

As cost pressure increases in the NHS the unit cost of implants is now being scrutinised, particularly with regard to cost effectiveness. The Press-Fit Condylar (PFC) Sigma implant can be used with either a conventional metal backed or alternatively an all polyethylene tibial component (part fitted to the shin bone), the latter considerably cheaper to manufacture. Four small prospective randomised trials and one large regional registry study with long follow up support the safe use of all polyethylene tibial components in TKA. The investigators will therefore undertake a prospective randomised controlled trial comparing the results of all polyethylene tibial components with those of conventional metal backed tibial components in patients aged 75 or over, comparing both clinical outcome and radiological survivorship.

The type of knee replacement used for each patient (metal-backed or polyethylene) will be chosen at random once a patient has agreed to take part in the study.

Data will be collected by means of follow-up appointments and questionnaires and clinical tests both before the operation 1 year, 2 years and 5 years postoperatively. This will allow us to see how both types of knee replacement perform over time and if one performs better than the other in terms of patients movement, pain and functional activities.

详细描述

Summary of design and methodology.

When a patient who is appropriate for the study is added to the waiting list for a Total Knee replacement they will be given (or if missed, posted) an information sheet about the study. This will allow patients several weeks to read the information and telephone the Orthopaedic research department, if they wish, with any questions they may have.

The Patients will then come to preassessment clinic as usual. At this point the study will be explained again in person, the patient will be given time to ask questions and will be asked if they wish to consent to participating.

If the patient consents to taking part they will complete preoperative measures and questionnaires There are 3 questionnaires on how the patient is functioning. 2 are completed by the patient and 1 with the help of the Researcher

The questionnaires are:

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 (Outcomes Assessor)

入排标准

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

入选标准

  • Patients suitable for simple cemented primary knee arthroplasty
  • Patients presenting with osteoarthritis of the knee
  • Patients with inflammatory arthropathy, requiring total knee arthroplasty
  • Patients must be ambulatory at time of preoperative assessment clinic
  • Patients must be able to understand instructions and be willing to return for follow up
  • Patients aged 75 years or over at the time of surgery

排除标准

  • Previous knee surgery (except arthroscopic / open meniscectomy)
  • Patients with significant medical co-morbidity
  • Disorders causing abnormal gait or significant pain
  • Patients unable to consent
  • Severe visual impairment

研究组 & 干预措施

All-polyethylene Tibial component

Active Comparator

Sigma PFC All polyethylene Tibial component will be implanted

干预措施: Sigma PFC (Device)

Metal Backed Tibial component

Active Comparator

Sigma PFC metal-backed tibial component will be implanted

干预措施: Sigma PFC (Device)

结局指标

主要结局

American Knee Society Score

时间窗: 5 year outcomes

次要结局

未报告次要终点

研究者

发起方
Maidstone & Tunbridge Wells NHS Trust
申办方类型
Other
责任方
Principal Investigator
主要研究者

Helen Samuel

Mr Nick Bowman- Consultant Orthopaedic Surgeon

Maidstone & Tunbridge Wells NHS Trust

研究点 (2)

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