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临床试验/NCT06145828
NCT06145828招募中不适用

Clinical Application of Cytokine Adsorption Technology in AIDS Patients With Severe Pneumonia and/or Septic Shock: An Observational Study.

Guangzhou 8th People's Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年10月23日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60
试验地点
1
主要终点
Mortality rate

研究概览

简要总结

Observing the Real-World Application Effectiveness of Cytokine Immune Adsorption Technology in AIDS Patients with Severe Pneumonia or septic shock.

详细描述

This is a prospective, single-center, non-randomized, clinical observational cohort study primarily focused on observing the clinical effects of cytokine adsorption technology in patients with AIDS complicated by severe pneumonia and/or septic shock. Based on the real-world application of cytokine adsorption technology in AIDS patients with severe pneumonia or septic shock, the study divides patients into two groups: one receiving cytokine adsorption combined with standard treatment, and another receiving standard treatment only. The study aims to observe the impact of these two different treatment strategies on clinical outcomes.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Confirmed HIV infection;
  • Progression to AIDS stage: CD4+ count <200 cells/ul and/or occurrence of AIDS opportunistic infections;
  • Age between 18 and 65 years;
  • Meeting the diagnosis of severe pneumonia or septic shock:
  • The criteria for severe pneumonia diagnosis refer to the 2021 ATS (American Thoracic Society) and IDSA (Infectious Diseases Society of America) guidelines for the treatment of community-acquired pneumonia;
  • The criteria for septic shock refer to the Chinese Society of Critical Care Medicine's "Chinese Guidelines for the Emergency Treatment of Sepsis/Septic Shock (2018).

排除标准

  • Coexisting central nervous system lesions, severe liver disease, or cirrhosis;
  • Concurrent AIDS-related or unrelated tumors;
  • Women who are pregnant or breastfeeding;
  • Severe underlying diseases of the heart, lungs, liver, kidneys, etc.;
  • Alcohol abuse or drug use;
  • The researcher believes that the overall condition of the subject affects the evaluation and completion of the trial.

结局指标

主要结局

Mortality rate

时间窗: 4 weeks

Compare the mortality rates of the cytokine adsorption combined with standard treatment group and the standard treatment group.

次要结局

  • Improvement in critical care scoring(Baseline and during treatment at weeks 1, 2, 3, 4.)

研究者

发起方
Guangzhou 8th People's Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Linghua LI

Chief physician

Guangzhou 8th People's Hospital

研究点 (1)

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