此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Dynamic Alterations of Th2/Th1 With New Onset of Community-acquired Severe Sepsis Patients

2018年8月19日 更新者:Jianfeng Xie

Dynamic Alterations of Th2/Th1 With New Onset of Community-acquired Severe Sepsis

To evaluate the dynamic alterations of Th2/Th1 for the prediction of clinical immunity and how it was related to 28 day-prognosis and ICU-acquired infections among critically ill patients of community-acquired severe sepsis with new onset.

研究概览

地位

完全的

条件

研究类型

观察性的

注册 (实际的)

85

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

    • Jiangsu
      • Nanjing、Jiangsu、中国、210000
        • Zhongda hospital

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 90年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

We enroll patients with community-acquired severe sepsis and then the patients admitted to ICU without the diagnosis of severe sepsis as ICU control group, and the heathy volunteers as healthy control group.

描述

For community-acquired severe sepsis group:

Inclusion Criteria:

  • at least 18 years of age and no more than 90 years of age
  • sepsis was defined according to consensus criteria
  • diagnosis of sepsis and complicatied with organ dysfunction no longer than 48 h
  • provided written informed consent.

Exclusion Criteria:

  • diagnosis of hematological,immunological disease or cancer
  • treatment with chemotherapy agents or corticosteroids within 6 months prior to or during the hospitalization

For non-severe sepsis ICU control group:

Inclusion Criteria:

  • at least 18 years of age and no more than 90 years of age
  • without diagnosis of sepsis and admitted to ICU
  • provided written informed consent.

Exclusion Criteria:

  • diagnosis of hematological,immunological disease or cancer
  • treatment with chemotherapy agents or corticosteroids within 6 months prior to or during the hospitalization

For healthy control group:

Inclusion Criteria:

  • at least 18 years of age and no more than 90 years of age
  • provided written informed consent.

Exclusion Criteria:

  • diagnosis of hematological,immunological disease or cancer
  • treatment with chemotherapy agents or corticosteroids within 6 months prior to enrollment

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
Comunity-acquired severe sepsis patients
Patients with new-onset community-acquired severe sepsis within 24h without confounding factors in immune status
Non-severe sepsis patients
Patients between 18 and 90 years of age and be admitted to the ICU without a diagnosis of severe sepsis.
Healthy controls
Heathy vonlunteers between 18 and 90 years of age.

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
Th2/Th1 upon enrollment
大体时间:Day 0 after enrollment for community-acquired severe sepsis group and Day 0 after enrollment for the non-severe sepsis patients and heathy control group
The blood samples were collected for T helper 1 cells and T helper 2 cells populations measured by flow cytometry. All groups are needed.
Day 0 after enrollment for community-acquired severe sepsis group and Day 0 after enrollment for the non-severe sepsis patients and heathy control group
Th2/Th1 on Day 3
大体时间:Day 3 after enrollment for community-acquired severe sepsis group
populations measured by flow cytometry. Only community-acquired severe sepsis group is needed.
Day 3 after enrollment for community-acquired severe sepsis group
Th2/Th1 on Day 7
大体时间:Day 7 after enrollment for community-acquired severe sepsis group
populations measured by flow cytometry. Only community-acquired severe sepsis group is needed.
Day 7 after enrollment for community-acquired severe sepsis group

次要结果测量

结果测量
大体时间
28-day mortality for community-acquired severe sepsis group
大体时间:28-day
28-day
ICU-acquired infection for community-acquired severe sepsis group
大体时间:28-day
28-day

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。

赞助

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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 (实际的)

2014年9月1日

初级完成 (实际的)

2018年7月20日

研究完成 (实际的)

2018年8月1日

研究注册日期

首次提交

2016年8月25日

首先提交符合 QC 标准的

2016年8月25日

首次发布 (估计)

2016年8月30日

研究记录更新

最后更新发布 (实际的)

2018年8月21日

上次提交的符合 QC 标准的更新

2018年8月19日

最后验证

2018年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • 2014ZDSYLL087.0

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.

订阅