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临床试验/NCT04268342
NCT04268342进行中(未招募)不适用

Gonorrhoea Resistance Assessment by Nucleic Acid Detection: A Program Evaluation

The University of Queensland2 个研究点 分布在 1 个国家目标入组 1,626 人开始时间: 2022年4月26日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
1,626
试验地点
2
主要终点
Change in ceftriaxone use

研究概览

简要总结

Three sexual health clinical services across Australia and their associated pathology testing laboratories are implementing a new management program for gonorrhoea infection. The services are implementing the use of gonorrhoea drug resistance testing as part of routine clinical and laboratory practice, where drug resistance test results are provided to clinicians quickly to guide choice of antibiotic therapy. Clinicians will identify gonorrhoea infection that is ciprofloxacin susceptible so that it can be treated with ciprofloxacin therapy, rather than ceftriaxone.

详细描述

This study aims to demonstrate the feasibility of a new approach to antibiotic stewardship based on individually tailored antibiotic prescribing. Three sexual health clinical services in New South Wales Australia with high caseloads of gay and bisexual men will adopt a new management practice for gonorrhoea infection involving provision of tailored antibiotic therapy by clinicians at the time of gonorrhoea diagnosis and treatment, guided by the results of resistance testing. The services are implementing the use of gonorrhoea drug resistance testing as part of routine clinical and laboratory practice, where drug resistance test results are provided to clinicians quickly to guide choice of antibiotic therapy. This differs from existing practice where the prolonged turn-around times for drug resistance testing results mean clinicians must prescribe drug therapy without knowing these results. This can lead to increasing levels of drug resistance to ceftriaxone.

The drug resistance test used in the new program detects genetic material (nucleic acids). It was developed and validated in Australia and is as accurate as existing culture-based drug resistance testing but provides quicker results. Patients treated presumptively at their first clinic visit will be treated with standard of care ceftriaxone. However, for cases treated at the return visit, clinicians will identify gonorrhoea infection that is ciprofloxacin susceptible so that it can be treated with ciprofloxacin therapy, rather than ceftriaxone. This will preserve ceftriaxone for situations where it must be used as the only effective drug available. Established patient follow-up procedures at clinical services will confirm that treatment has been successful.

Quantitative data from the clinical and laboratory services in the study will be used to assess the proportion of all cases treated with ceftriaxone. The cure rate in gonorrhoea cases within the new management program versus standard care will also be assessed which will help illustrate the impact of the new management program.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
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 diagnosed with gonorrhoea infection at the return visit

排除标准

  • Patients for whom ciprofloxacin is contraindicated

结局指标

主要结局

Change in ceftriaxone use

时间窗: 12 months after implementation commences

The proportion of gonorrhoea cases treated at the return visit with ceftriaxone

次要结局

  • Acceptability(1-12 months after implementation commences)
  • Cost effectiveness(12 months after implementation commences)
  • Cure rate(At 12 months after implementation commences)
  • Process evaluation(12 months after implementation commences)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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