Detecting Infections Rapidly and Easily for Bacteremia Trial (DIREBT) (DIREBT)
2015年9月25日 更新者:T2 Biosystems
Detecting Infections Rapidly and Easily for Bacteremia Trial (DIREBT)-Part I (Prospective Collection and Freezing of Whole Blood Specimens)
To assure the uniform collection, handling, storage and transport of patient whole blood specimens and associated information to support validation of the T2 Bacteremia Assay.
研究概览
地位
完全的
条件
详细说明
This protocol is intended for use by external sites collecting clinical research specimens for T2 Biosystems' use in developing the T2Bacterial Assay.
Specimens and information on patients' medical history, blood properties, medications, and blood culture history/results are required from the T2Bacterial Assay's target patient population (i.e., candidates for blood culture).
Ideally, clinical specimens for use in developing the T2Bacterial Assay will be collected from negative blood culture, positive non-bacteria blood culture and positive bacteria blood culture patients.
研究类型
观察性的
注册 (实际的)
156
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
New Jersey
-
Camden、New Jersey、美国、08103
- Cooper Medical School
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 95年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
取样方法
非概率样本
研究人群
Patients with blood culture results are eligible to participate
描述
Inclusion Criteria:
- Subject or subject's authorized representative must be able to understand, read and sign the study specific informed consent form after the nature of the study has been fully explained to them.
- Males and females 18 - 95 years of age.
For Group A,
- Subject is confirmed to have bacteremia (gram negative rods, gram negative coccobacillus, and/or gram positive cocci) as evidenced by a positive diagnostic blood culture
- Subsequent species identification identifies the presence of one of the following 6 species of bacteria:
- Acinetobacter baumannii
- Staphylococcus aureus
- Klebsiella pneumonia
- Pseudomonas aeruginosa
- Enterococcus faecalis
- Enterococcus faecium
For Group B,
- Males and females 18 - 95 years of age.
- Subject is confirmed to not have bacteremia from the 6 bacteria species targeted by this study, as evidenced by diagnostic blood culture and subsequent species identification.
Exclusion Criteria:
- Use of any novel (i.e. not commercially available) drug compound within 30 days prior to the collection of T2 blood specimens.
- Subject has other co-morbid condition(s) that, in the opinion of the Investigator, could limit the subject's ability to participate in the study or impact the scientific integrity of the study.
- Subject has had an anti-bacterial drug administered through the same port or central line as is used to collect the clinical research specimens. A line draw cannot be used to obtain a study sample if an antibacterial agent was administered intravenously within the last 72 hours, unless the site can specifically document that a different line was used to administer the anti-bacterial agent.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
|---|
|
Bacteremia Positive Patients
Symptomatic adult patients, confirmed via diagnostic blood culture and species identification followed by subsequent second blood culture results and species identification that are positive for each of the following species of bacteria (Target 6 Species).
|
|
Bacteremia Negative Patients
Adult patients confirmed via diagnostic blood culture and species identification and subsequent second blood culture and species identification as being negative for the Target 6 species
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of bacteremia positive patients
大体时间:3-5 days post blood culture
|
Number of bacteria positive patients based on concordant, sequential blood culture results and a positive T2 signal
|
3-5 days post blood culture
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of bacteremia negative patients
大体时间:3-5 Days post blood culture
|
Number of negative bacteremia samples based on concordant, sequential blood culture results and a negative T2 signal
|
3-5 Days post blood culture
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2013年8月1日
初级完成 (实际的)
2015年8月1日
研究完成 (实际的)
2015年8月1日
研究注册日期
首次提交
2013年8月7日
首先提交符合 QC 标准的
2013年8月7日
首次发布 (估计)
2013年8月9日
研究记录更新
最后更新发布 (估计)
2015年9月28日
上次提交的符合 QC 标准的更新
2015年9月25日
最后验证
2015年9月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.