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临床试验/NCT02782013
NCT02782013已完成不适用

Study of Progression of Hospitalized Community Acquired Pneumonia - Genetic Resistance and Susceptibility for the Evolution of Severe Sepsis

Pneumonia Research Network on Genetic Resistance and Susceptibility for the Evolution of Severe Seps64 个研究点 分布在 2 个国家目标入组 2,309 人开始时间: 2009年8月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
2,309
试验地点
64
主要终点
Worst measure of disease severity

研究概览

简要总结

Pneumonia is a common infectious disease of the lung, often requiring treatment in the hospital. Clinical scoring systems are available, identifying patients not requiring hospitalization. However, the course of disease of patients in the hospital remains hard to predict. While most patients will recover quickly, some will, despite appropriate treatment, develop a severe course leading to sepsis and systemic responses resulting in organ dysfunction. The PROGRESS study aims to identify clinical, genetic, and other molecular markers and combinations thereof predicting a severe course of pneumonia in the hospital. Such predictors will, for instance, support decisions on earlier transfer of patients to intensive care and thus improving outcome.

详细描述

Pneumonia is a common infectious disease of the lung, often requiring treatment in the hospital. Clinical scoring systems are available, identifying patients not requiring hospitalization. However, the course of disease of patients in the hospital remains hard to predict. While most patients will recover quickly, some will, despite appropriate treatment, develop a severe course leading to sepsis and systemic responses resulting in organ dysfunction. The PROGRESS study aims to identify clinical, genetic and other molecular markers and combinations thereof predicting a severe course of pneumonia in the hospital. Such predictors will, for instance, support decisions on earlier transfer of patients to intensive care and thus improving outcome.

The PROGRESS study was initially approved by the ethics board of the University Hospital Jena, Friedrich-Schiller-University Jena, Germany (2403-10/08, November 6th, 2008) and subsequently by the ethics committees of all recruiting study centers.

In this observational, longitudinal case-cohort study, patients are enrolled within 48 hours of hospitalization and patient's progress is followed in much detail for up to six days thereafter. Further data are collected until discharge from the hospital. Patients are followed up on at days 28, 180, and 360 after enrollment.

Baseline assessment comprises sociodemographic, anamnestic, family history, and live style information. Upon enrollment, Pneumonia Severity Index (PSI) and CURB-65 are determined. For the day of enrollment and up to six subsequent study days routine laboratory and clinical observations and information on therapy are documented as well as data for determining the Sequential Organ Failure Assessment (SOFA) score, Systemic Inflammatory Response Syndrome (SIRS) status, and organ dysfunction. Starting with enrollment, up to six consecutive sets of biomaterials are collected comprising serum, plasma, and materials for extraction of RNA. Blood for extraction of DNA is collected once.

Follow up comprises vital status, housing situation, recurrence of pneumonia, and a quality of life questionnaire.

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

  • Hospitalization with community acquired pneumonia (CAP) confirmed by pulmonary infiltrate in chest radiograph
  • Working diagnosis of CAP by enrolling physician
  • Adult patient >= 18 years of age
  • Valid informed consent form
  • At least 2 out of the five following clinical symptoms:
  • Purulent sputum
  • Shortness of breath or need for respiratory support
  • Crackling or rales on auscultation, dullness to percussion, or bronchial breathing

排除标准

  • Participation in this study at an earlier time
  • Hospitalization for any reason within 28 days prior to hospitalization for the current episode of CAP
  • More than 48 hours in the hospital before enrollment
  • Breastfeeding
  • Decision on limitation of therapy before enrollment
  • Known HIV infection or AIDS
  • Anti-tumor treatment within the past six months
  • Post-stenotic pneumonia in conjunction with bronchial carcinoma
  • Therapy with corticosteroids ≥ 20mg for ≥ 14 days before enrollment
  • Non-steroidal immunosuppressive therapy within the past six months
  • Cytostatic therapy within the past six months
  • Radiation therapy within the past six months
  • Bone marrow transplant received
  • Respiratory support at home via tracheostoma
  • Cystic fibrosis
  • Active tuberculosis
  • Acute lung injury or acute respiratory distress syndrome for extrapulmonary reasons
  • Massive aspiration
  • Sepsis with extrapulmonary focus
  • Acute pulmonary embolism
  • Congestive heart failure New York Heart Association (NYHA) IV stadium
  • Liver insufficiency Child-Pugh C stadium

结局指标

主要结局

Worst measure of disease severity

时间窗: Between enrollment and day six

Disease severity is operationalized by the Sequential Organ Failure Assessment (SOFA-score).

次要结局

  • duration of hospitalization(up to one year after enrolment)
  • All cause mortality(up to one year after enrolment)
  • disease-specific mortality(up to one year after enrolment)
  • duration of intensive care treatment(up to one year after enrolment)
  • duration of ventilator assisted breathing(up to one year after enrolment)

研究者

发起方
Pneumonia Research Network on Genetic Resistance and Susceptibility for the Evolution of Severe Seps
申办方类型
Other
责任方
Sponsor

研究点 (64)

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