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临床试验/NCT02225821
NCT02225821已完成4 期

Antibiotic Prophylaxis to Prevent Wound Infections Following Implant Removal

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)21 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2014年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
500
试验地点
21
主要终点
Postoperative wound infection (POWI)

研究概览

简要总结

In the Netherlands about 18,000 surgical procedures with implant removal are annually performed after fracture healing, of which 30-80% concern the foot, ankle and lower leg region. For clean surgical procedures, the rate of postoperative wound infections (POWIs) should be less than 5%. However, rates of 10-12% following implant removal, specifically after foot, ankle and lower leg fractures are reported. Currently, surgeons decide individually if antibiotics prophylaxis is given, since no guideline exists. This leads to undesirable practice variation.

Therefore, the investigators propose a double-blind randomized controlled trial (RCT) in patients scheduled for implant removal following a foot, ankle or lower leg fracture, to assess the (cost-)effectiveness of a single gift of antibiotic prophylaxis. Primary outcome is a POWI within 30 days after implant removal. Secondary outcomes are quality of life, functional outcome at 30 days and 6 months after implant removal and costs.

With 2 x 250 patients a decrease in POWI from 10% to 3.3% (expected rate in clean-contaminated elective orthopedic trauma procedures) can be detected (Power=80%, 2-sided alpha=5%, including 15% lost to follow up).

If the assumption of the investigators, that prophylactic antibiotics prior to implant removal reduces the infectious complication rate, is confirmed by this RCT, this will offer a strong argument to adopt a single gift of antibiotic prophylaxis as standard practice of care. This will reduce the incidence of POWIs and consequently will lead to less physical and social disabilities and health care use. In addition, it will decrease the rate of use of empiric broad-spectrum antibiotics (and antibiotic resistance) prescribed upon suspicion or diagnosis of a POWI. A preliminary, conservative estimation suggests yearly cost savings in the Netherlands of €3.5 million per year.

详细描述

See study protocol

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients ≥18 years and ≤75 years of all ethnic backgrounds
  • Implant removal following foot, ankle and/or lower leg surgery

排除标准

  • Removing and re-implanting osteosynthesis material in the same session
  • Active wound infection or (plate) fistula
  • Antibiotic treatment at time of elective implant removal for a concomitant disease or infection
  • A medical history of an allergic reaction to a cephalosporin, penicillin, or any other β-lactam antibiotic.
  • Insufficient comprehension of the Dutch language to understand the patient information to make an informed decision to participate.
  • Kidney disease (eGFR <60 ml/min/1.73m^2).
  • Treatment with probenecide, anticoagulants (see SPC)
  • Pregnancy and lactation

研究组 & 干预措施

antibiotic prophylaxis

Active Comparator

a single gift of 1000 mg cefazolin in 10 cc of NaCl 0.9% (intervention group)

干预措施: Cephalozin (Drug)

No antibiotic prophylaxis

Placebo Comparator

a single gift of 10 cc NaCl 0.9%, given in the same manner (control group).

干预措施: Sodium chloride (Other)

结局指标

主要结局

Postoperative wound infection (POWI)

时间窗: 30 days

The primary outcome variable is a POWI within 30 days after implant removal as defined by the criteria applied by the Centers for Disease and Control.

次要结局

  • Health-related quality of life(baseline, one month, 6 months)
  • Functional outcome(baseline, 1 month, 6 months)
  • Patient satisfaction(1 month, 6 months)
  • Health care resources utilization(baseline, 1 month, 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

J.C. Goslings

Prof. Dr.

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

研究点 (21)

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