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Clinical Trials/ChiCTR2200058375
ChiCTR2200058375
Not yet recruiting
Not Applicable

脓毒症短期预测预后模型建立及外部验证

1 site in 1 country54 target enrollmentStarted: April 1, 2022Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
54
Locations
1
Primary Endpoint
28 天的生存情况

Overview

Brief Summary

构建和验证一个简单易施的评分工具,用于急诊成人脓毒症患者短期预后生存情况。

Study Design

Study Type
预后研究
Primary Purpose
队列研究

Eligibility Criteria

Ages
18 to 100 (—)
Sex
All

Inclusion Criteria

  • 1.根据《脓毒症和脓毒症休克国际共识第三版(Sepsis-3)指南》确诊为脓毒症;

Exclusion Criteria

  • 1.长期应用激素、免疫抑制剂;
  • 2.存在血液系统疾病;
  • 3.恶性肿瘤或恶性病质;
  • 4.妊娠及哺乳期妇女。

Arms & Interventions

存活组和非存活组

Outcomes

Primary Outcomes

28 天的生存情况

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor

Study Sites (1)

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