EUCTR2008-004807-67-GR进行中(未招募)不适用
AN OPEN-LABEL, NON-RANDOMIZED PHASE IV CLINICAL TRIAL OF THE EFFICACY OF INTRAVENOUSLY ADMINISTERED 1000MG PARACETAMOL AS ANTIPYRETIC AND ANALGESIC MEDICATION - ?NTRAVENOUS 1000MG PARACETAMOL AS ANTIPYRETIC AND ANALGESIC MEDICATIO
niversity of Athens, Medical School0 个研究点开始时间: 2009年2月18日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
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
- •Age greater than or equal to 18 years
- •Written informed consent by the patients
- •Medical condition necessitating the administration of antipyretic or analgesic medications
- •Are the trial subjects under 18? no
- •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
- •?ge lower than 18 years
- •Lack of informed consent
- •History of liver cirrhosis
- •Blood creatinine greater than 3mg/dl
- •Blood AST greater than 3 times the upper normal level according to the lab of the participating hospital
- •History of hypersensitivity to non-steroidal ant-iinflammatory drugs
- •History of abuse of analgesics
- •Pregnancy or lactation
- •Fulminant hemorrhage of the upper or lower digestive tract
- •Thrombocytopenia defined as less than 50000 platelets/µl
研究者
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