EUCTR2017-001406-15-ES进行中(未招募)1 期
Adequate duration of antibiotic treatment in community acquired pneumonia categorized by pneumonia severity index (PSI)
Fundació Clínic per la Recerca Biomèdica0 个研究点目标入组 424 人开始时间: 2018年4月9日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 424
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
- •1) Hospitalized patients diagnosed with Community Acquired Pneumonia: appearance of a new radiological infiltrate plus the presence of at least two of the following signs or symptoms: fever (> 38 ºC), cough, expectoration, chest pain, dyspnea or tachypnea, and signs of occupation of the alveolar space.
- •2) A PSI score class IV or V.
- •3) Patients who have received adequate antibiotic treatment according to clinical guidelines from the first hour of emergency room admission.
- •4) Patients who achieve clinical stability: temperature =37.2 ºC, heart rate =100 beats / min, respiratory rate =24 breaths / min, systolic blood pressure> 90 mmHg; oxygen saturation> 90%; or oxygen blood pressure> 60 mmHg (15) before the fourth day.
- •5) Signature of informed consent.
- •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 212
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 212
排除标准
- •1) Immunosuppression: Coinfection with HIV and presence of AIDS, neutropenic or have received immunosuppressive treatment for any cause. Patients with chronic use of corticosteroids (prednisone or its equivalent)> 10 mg / day for 14 days.
- •2) Patients hospitalized in the previous 14 days.
- •3) Suspected multi-resistant germs of any cause.
- •4) Hypersensitivity or alterations in the tendons associated with the fuoroquinolones.
- •5) Pregnancy or lactation
研究者
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