EUCTR2010-020083-38-IT进行中（未招募）不适用
A Multicenter, Study of the Safety of Oseltamivir Administered Intravenously for the Treatment of Influenza in Patients Aged = 13 Years. - ND
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Patients are eligible for the study if they meet all of the following criteria: • Male and female adults and adolescents, 13 years of age and older • Diagnosis of influenza by virology testing or clinical diagnosis based on symptoms suggestive of influenza • = 96 hours between the onset of influenza-like illness and first dose of study medication • Patient is willing and able to comply with study requirements and give consent, or, if applicable, consent may be given by a parent, legal guardian or legal representative • Female patients who are pregnant may be enrolled only if the potential benefit justifies the potential risk to the fetus • Female patients who are lactating may be enrolled only if the potential benefit for the lactating mother justifies the potential risk to the breast-fed infant.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Patients meeting any of the following criteria are ineligible for participation in the study: • Patients with clinical evidence of severe hepatic decompensation at the time of randomization • Electrocardiogram showing acute ischemia or significant arrhythmia • Allergy to test medication • Patients taking probenicid medication within 7 days before starting study medication • Participation in a clinical trial or expanded access trial with an investigational drug in the 4 weeks prior to randomization.
研究者
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