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临床试验/NCT01079559
NCT01079559撤回3 期

The Effectiveness of Antibiotic Cement Compared to Regular Cement in Reducing the Rate of Infection Following Total Knee Arthroplasty: The ABC Feasibility Study

University of Western Ontario, Canada2 个研究点 分布在 1 个国家开始时间: 2010年3月3日最近更新:
适应症

试验速览

阶段
3 期
状态
撤回
发起方
试验地点
2
主要终点
relative risk of infection

研究概览

简要总结

Rationale: Infection following total knee replacement (TKA) is a devastating complication that usually requires prosthesis removal, hospitalization while the infection is eradicated, and a second surgery to implant a revision prosthesis. For primary TKA, prophylactic antibiotic-loaded cement (ABC) may not only reduce the rate of infection it may also reduce the rate of revisions due to implant loosening. Current controversy about the use of ABC exists around the world. Without a definitive trial, patients will be exposed to a treatment of uncertain efficacy that may cause antibiotic resistant bacterial strains and will certainly generate high costs to the healthcare system. Purpose: To determine, 1) the extent to which ABC compared to regular cement reduces the infection rate in patients over the first two years following TKA and, 2) the resource use implications associated with the use of ABC for TKA. Methods: This is a randomized clinical trial in which 8,800 patients with undergoing primary TKA are allocated to either Simplex™ P with Tobramycin or Simplex™ P bone cement. We will exclude patients with a prior joint infection, an allergy to tobramycin, and those with no fixed address. All patients will be administered IV antibiotics immediately prior to surgery. Patients and surgeons will be blind to group allocation. The primary outcome measure is infection. Follow-up visits will take place at 6 weeks and 3, 12 and 24 months postoperative. A blinded adjudicator will review all reported infections and determine whether the putative infection is a study event. Blinded radiologists will interpret the 2 year series of radiographs for each patient. We will compare the rates of infection and implant loosening between the two treatment groups using survival analyses. This study includes a full economic analysis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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

  • patients with osteoarthritis of the knee,
  • patients who are undergoing primary knee replacement,
  • patients who are able to provide informed consent.

排除标准

  • patients with a prior joint infection,
  • patients who have a known allergy to tobramycin, and
  • patients who have no fixed address.

结局指标

主要结局

relative risk of infection

时间窗: 6 weeks and 3, 12 and 24 months postoperative

patients suspected of having an infected total knee replacement in the post-operative period will be evaluated clinically, and will undergo lab evaluation and an aspiration

次要结局

  • patient-reported disease-specific health-related quality of life (HRQOL)(6 weeks and 3, 12 and 24 months postoperative)
  • cost-effectiveness(6 weeks and 3, 12 and 24 months postoperative)
  • radiographic evidence of prosthetic failure(6 weeks and 3, 12 and 24 months postoperative)

研究者

发起方
University of Western Ontario, Canada
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dianne Bryant

Associate Professor

University of Western Ontario, Canada

研究点 (2)

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