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临床试验/NCT03806166
NCT03806166已完成不适用

Short or Long Antibiotic Regimes in Orthopaedics (SOLARIO): A Randomised Open Label Multi-Centre Clinical Trial

Oxford University Hospitals NHS Trust43 个研究点 分布在 4 个国家目标入组 500 人开始时间: 2019年2月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
500
试验地点
43
主要终点
Definitive treatment failure (infection recurrence)

研究概览

简要总结

Research question: If adults with bone or joint infection have local antibiotic therapy, can they do without prolonged treatment with antibiotics by mouth (oral) or injection?

Adults with bone or joint infections are usually given long courses of oral antibiotics or into a vein (intravenous) following surgery. It is also safe to give antibiotics directly into the bone or joint at the time of surgery: this is called local antibiotic therapy. This study investigates whether using local antibiotic therapy would allow shorter courses of oral or intravenous antibiotics, in order to limit antibiotic resistance, side effects and cost.

This study compares short against long courses of oral or intravenous antibiotics for adults who have been given appropriate local antibiotic therapy to treat bone or joint infection. Patients who can take part will be randomly divided into two groups within 7 days of surgery. One group will stop oral or intravenous antibiotics, while the other group will continue for 4 weeks or more (standard treatment).

Adults with bone and joint infections who have already had surgery and local antibiotic therapy will be invited. Patients will not take part if they need intravenous antibiotics for another reason, or if their infection is caused by bacteria resistant to the antibiotic(s) used in their local antibiotic therapy.

Main measurement: how many patients' infections return within 12 months after surgery. This will be decided by a group of doctors who do not know what treatment the patient received.

Other important measurements: serious adverse events; side-effects; quality of life; cost of treatment.

Patients will be asked questions at their usual clinic visits, and will be given a questionnaire at the start of treatment and 1 year later.

详细描述

Using antibiotics wisely, only when and where they are really needed, is important to prevent superbugs emerging. At the moment, bone and joint infections are usually treated by a combination of surgery and antibiotics. Traditionally, treatment relies on several weeks of antibiotics as tablets or injections (systemic antibiotics), but these can sometimes cause problems.

It is now possible to administer local antibiotics at the time of surgery directly to the site of infection. This allows much higher levels of the antibiotic to be delivered, for days or weeks, following surgery. Therefore, this study will investigate whether local antibiotics with a shorter course of systemic antibiotics can treat bone and joint infections as effectively as local antibiotics with a prolonged course of systemic antibiotics (usual treatment). If so, it may be possible to reduce antibiotic side effects, help to prevent antibiotic resistant bacteria emerging and limit overall treatment costs.

Patients who agree to participate in this study will be allocated at random to two treatment strategies after surgery for bone and joint infection.

One group of patients will be treated with local antibiotics and a long course of systemic antibiotics, which is the usual treatment: this is the 'long group'.

The other group will be treated with local antibiotics and a short course of systemic antibiotics: this is the 'short group' whose treatment differs from the current usual treatment.

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)

盲法说明

Ascertainment of the primary outcome (treatment failure) will be undertaken by an independent committee of specialists, using redacted participant clinical records, who will remain unaware of the treatment allocation of the participant, and who will ascertain treatment failure according to established objective criteria.

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

  • Provision of informed consent
  • Aged 18 years or over
  • Presenting with an orthopaedic infection, defined by one or more of the following criteria:
  • localised pain, OR
  • localised erythema, OR
  • temperature ≥ 38.0 C, OR
  • a discharging sinus or wound
  • Undergoing surgical treatment for the infection
  • Locally administered antibiotic(s) at the site of orthopaedic infection
  • Has received <= 7 days of systemic antimicrobial therapy after surgery
  • Would ordinarily be managed with a prolonged course (>= 4 weeks) of systemic antibiotic(s)
  • Specimens for microbiological analysis taken at index surgery

排除标准

  • Surgical exclusion criteria
  • The index operation was not a definitive procedure with the aim of eradicating infection:
  • Primary closure has not been achieved, or
  • Re-look surgery is planned
  • The index operation involved implant retention (e.g. DAIR)
  • Microbiological exclusion criteria
  • Any identified micro-organisms from operative specimens from the site of incident infection are fully resistant to the local antibiotic(s) administered at the site of infection
  • Medical exclusion criteria
  • Other infection necessitating additional systemic antibiotic treatment beyond 7 days after surgery, such as Staphylococcus aureus bacteraemia, psoas abscess, discitis or bacterial endocarditis
  • If the patient is in a clinical trial involving an Investigational Medicinal Product (IMP) related to infection

结局指标

主要结局

Definitive treatment failure (infection recurrence)

时间窗: 12 months from the time of surgery for bone or joint infection

Proportion of participants in each treatment group experiencing definitive treatment failure (infection recurrence), ascertained by an independent committee of experts unaware of the treatment allocation of the participant, according to established criteria.

次要结局

  • Possible or probable treatment failure(12 months from the time of surgery for bone or joint infection)
  • Serious Adverse Events(12 months from the time of surgery for bone or joint infection)
  • Quality of life measured by EuroQol 5 Dimensions 5 Levels Score and EuroQol Visual Analogue Score(At baseline and 12 months from the time of surgery for bone or joint infection)
  • Antibiotic side effects(This will be assessed at baseline (pre-randomisation, at <7 days of treatment), 6 weeks and 3 months from the time of surgery for bone or joint infection)

研究者

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

Matthew Scarborough

Principle Investigator, Consultant in Clinical Infection.

Oxford University Hospitals NHS Trust

研究点 (43)

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