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临床试验/NCT07357935
NCT07357935尚未招募1 期

Early Inflammatory-Immune Stratification and Precision Glucocorticoid Intervention in Acute Respiratory Failure Induced by Community-Acquired Pneumonia

Qingyuan Zhan0 个研究点目标入组 500 人开始时间: 2026年2月1日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
500

研究概览

简要总结

This is a prospective, multicenter, interventional cohort study aimed at constructing a high-quality, dynamic multimodal database for patients with acute respiratory failure caused by community-acquired pneumonia (CAP-ARF). The study focuses on bacterial CAP-ARF patients receiving standardized glucocorticoid therapy to investigate the heterogeneity of treatment responses under different etiologies and immune statuses. The goal is to provide a data foundation for precise immune stratification and identification of glucocorticoid-sensitive populations.

详细描述

This study is part of the National Major Science and Technology Project for the Prevention and Control of Emerging and Major Infectious Diseases. It integrates existing multicenter cohorts (including healthy individuals, non-infectious ARF, mild CAP, and CAP-ARF patients) and establishes a prospective, standardized glucocorticoid intervention cohort for bacterial CAP-ARF. Eligible patients (age ≥18, admitted to ICU ≤48 hours, meeting bacterial pneumonia and severe ARF criteria) are treated with methylprednisolone based on initial oxygenation index (PFR ≤150 mmHg: 1 mg/kg/d; PFR >150 mmHg: 0.5 mg/kg/d). Dosing is adjusted at day 4 based on clinical response (improvement in oxygenation and SOFA score), with a total treatment duration of 7 days. Multimodal data-including clinical information, inflammatory/immune biomarkers, chest CT imaging, and multi-omics sequencing (transcriptomics, proteomics, metabolomics)-are collected at multiple timepoints (baseline, day 4, day 8). The database will support the analysis of immune-inflammatory profiles, identification of glucocorticoid-responsive subgroups, and development of precision intervention strategies for CAP-ARF.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • Age ≥ 18 years.
  • Admitted to the Intensive Care Unit (ICU) within 48 hours.
  • Meet diagnostic criteria for bacterial community-acquired pneumonia (CAP).
  • Meet at least one severity criterion: a) Receiving mechanical ventilation for acute respiratory failure with PEEP ≥ 5 cmH2O; OR b) On high-flow oxygen with FiO2 ≥ 0.5 and PaO2/FiO2 ratio ≤ 250 mmHg; OR c) On a reservoir oxygen mask with PaO2 below the specified flow threshold (see protocol).
  • Signed informed consent.

排除标准

  • Suspected aspiration pneumonia.
  • Invasive mechanical ventilation within 14 days prior to admission.
  • Diagnosis of hospital-acquired or ventilator-associated pneumonia (HAP/VAP).
  • Positive for influenza virus, active tuberculosis, or fungal infection (except Pneumocystis jirovecii).
  • Active viral hepatitis or herpesvirus infection.
  • Hypersensitivity to glucocorticoids, or contraindications as judged by the investigator (e.g., severe concurrent infections, active gastrointestinal hemorrhage).
  • High-dose glucocorticoid therapy (>1 mg/kg/day prednisone equivalent) within 30 days for underlying disease.
  • Death within 24 hours of ICU admission.
  • Pregnancy or lactation.
  • Participation in other interventional studies or refusal to participate.

研究者

发起方
Qingyuan Zhan
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Qingyuan Zhan

Director

China-Japan Friendship Hospital

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