EUCTR2013-000469-35-NO进行中(未招募)不适用
Peroral antibiotic treatment of endocarditis - POET
Hillerød Hospital0 个研究点目标入组 400 人开始时间: 2013年5月15日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 400
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
- •Patient admitted to hospital with a diagnosis of left-sided endocarditis as evaluated by a project responsible physician in one of the study sites:
- •-A diagnosis of endocarditis as evaluated by the Duke criteria
- •- Endocarditis with any of the following bacteria:
- •- streptococci
- •-staphylococci
- •-enterococci
- •-Patients >=18 years
- •-Patient has received at least 10 days of correct intravenous antibiotic treatment for bacterial endocarditis, or at least 7 days treatment after surgical intervention
- •-At least 10 days of the antibiotic therapy is left
- •-Temperatur <=37.5 C for 2 days
- •-Decline in blood inflammation parameters (serum-CRP at least 75% comparing peak-value or<;4 x upper limit of normal, and leucocytes at least 25% of peak-value or 15 mia/L) during the antibiotic treatment
- •-No signs of abscess or any worsening of valve function as assessed by transthoracal or transoesophageal ekkocardiography<;48 hours prior to randomisation
- •-Patients that beside the above mentioned also fulfill the modified OPAT (out-patient antibiotic therapy) criteria may be included in the part of the study concerning ambulatory therapy
- •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 15
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 35
排除标准
- •Previous endocarditis within the last year with the same bacteria
- •(endocarditis-relapse)
- •-Body mass index >40 kg/m2
- •-Heart surgery planned within 6 weeks from randomisation
- •-Any other concurrent infection that needs intravenous antibiotic
- •-Any abdominal/ bowel disease that may reduce uptake of oral
- •- Known reduced immunocompetence such as HIV, or treatment with chemotherapeutics or prednisolon >20mg/day
- •-Subjects incapable of giving informed consent
- •-Subjects with low complience included inravenous drug users
研究者
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