跳至主要内容
临床试验/NCT06479421
NCT06479421招募中不适用

A Clinical Study for Developing AI-based Clustering Model for Personalized Medicine in Acute Respiratory Failure: Single Center, Prospective Cohort Study

Samsung Medical Center2 个研究点 分布在 2 个国家目标入组 250 人开始时间: 2023年8月14日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
250
试验地点
2
主要终点
Hospital Mortality

研究概览

简要总结

The investigators will prospectively collect clinical information to develop a clustering analysis model and confirm phenotype for patients with acute respiratory failure who admit to the intensive care unit and require oxygen supply beyond a high flow nasal cannula, and a control group without acute respiratory failure. and clinical characteristics and prognosis will be compared.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • # Inclusion Criteria:
  • - Acute Respiratory Failure group
  • Among patients admitted to the internal medicine intensive care unit at Samsung Seoul Hospital, if all of the following conditions are met:
  • 1) Age 18 or older 2) Patients who require treatment with high flow nasal cannula (HFNC), non-invasive ventilation (NIV (BIPAP or CPAP)), or mechanical ventilation (MV) due to acute respiratory failure.
  • - control group For comparative analysis, among patients admitted to the internal medicine intensive care unit at Samsung Seoul Hospital who meet all of the following conditions, they are registered as a control group with the consent of the subjects and undergo the same research procedure.
  • Age 18 or older
  • Patients who do not require high flow nasal cannula (HFNC), non-invasive ventilation (NIV (BIPAP or CPAP)), or mechanical ventilation (MV) treatment

排除标准

  • If any of the following criteria applies, participants will not be permitted to participate in this clinical trial.
  • Patients 48 hours after oxygen treatment (HFNC, NIV (BIPAP or CPAP), MV)
  • Patients transferred from another hospital
  • Patients with limitations in treatment

研究组 & 干预措施

Acute Respiratory Failure group

Among patients admitted to the internal medicine intensive care unit at Samsung Seoul Hospital, if all of the following conditions are met:

  1. Age 18 or older
  2. Patients who require treatment with high flow nasal cannula (HFNC), non-invasive ventilation (NIV (BIPAP or CPAP)), or mechanical ventilation (MV) due to acute respiratory failure.

Control group

For comparative analysis, among patients admitted to the internal medicine intensive care unit at Samsung Seoul Hospital who meet all of the following conditions, they are registered as a control group with the consent of the subjects and undergo the same research procedure.

  1. Age 18 or older
  2. Patients who do not require high flow nasal cannula (HFNC), non-invasive ventilation (NIV (BIPAP or CPAP)), or mechanical ventilation (MV) treatment

结局指标

主要结局

Hospital Mortality

时间窗: From date of admission until the date of hospital discharge or date of death from any cause, whichever came first, assessed up to 1 year

clinical outcomes - Hospital Mortality

次要结局

  • ICU Mortality(From date of ICU admission until the date of ICU discharge or date of death from any cause, whichever came first, assessed up to 6 months)
  • ICU length of stay(From date of ICU admission until the date of ICU discharge, assessed up to 6 months)
  • Hospital length of stay(From date of hospital admission until the date of hospital discharge, assessed up to 1 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ryoung-Eun Ko

Clinical assistant professor

Samsung Medical Center

研究点 (2)

Loading locations...

相似试验