NL-OMON48253已完成不适用
Target attainment of ciprofloxacin as infection prophylaxis during chemotherapy-induced neutropenia in patients treated for haematological malignancies. - Target attainment of ciprofloxacin as infection prophylaxis.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 46
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •Receiving ciprofloxacin orally or intravenously as prophylaxis as part of
- •standard care prescribed by the treating physician
- •Admitted to the nursing ward of the haematology department or to another
- •general ward, but treated for a haematological malignancy
- •Age * 18 years
- •Informed consent is obtained
排除标准
- •Admitted to the Intensive Care Unit
- •Receiving RRT (i.e. haemodialysis, peritoneal dialysis, continuous venovenous
- •hemofiltration or another ways of RRT) during ciprofloxacin prophylaxis
- •Patients with cystic fibrosis
- •Severely burned patients, defined as a burned surface * 10%
- •Incapacitated patients, i.e. a minor or legally incompetent adult
- •Informed consent is not obtained
研究者
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Target attainment of ciprofloxacin as infection prophylaxis during chemotherapy-induced neutropenia in patients treated for haematological malignancies.All patients receiving ciprofloxacin prophylaxis as standard care will be included, regardless of treatment with different cytostatic agents, regardless of the severity of adverse effects of the treatment (in particular mucositis) and regardless of the degree and duration of neutropenia, as long as ciprofloxacin is recommended as infection prophylaxis within the applied treatment protocol.NL-OMON20490Amsterdam UMC - location Academic Medical Centre (AMC), University of Amsterdam46
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