跳至主要内容
临床试验/NL-OMON45194
NL-OMON45194已完成不适用

Reduction of antibiotic therapy by biomarkers in patients with CAP episodes - REDUCE study

Medisch Centrum Alkmaar0 个研究点目标入组 468 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
468

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Male and female patients with a diagnosis of CAP and all criteria listed below:
  • 1. Age 18 or above, no upper age limit will be employed.
  • 2. Patients must require hospitalisation.
  • 3. Clinical presentation of an acute illness with one or more of the following symptoms:
  • a. Temperature * 38.0 *C (100.4°F)
  • b. Dyspnoea
  • c. Cough (with or without expectoration of sputum)
  • d. Chest pain
  • e. Hemoptysis
  • f. Malaise or fatigue
  • h. Gastro-intestinal symptoms
  • i. Rales, rhonchi or wheezing
  • j. Egophony or bronchial breath sounds
  • 4. New consolidation(s) on the chest radiograph.
  • 5. Written informed consent obtained.
  • 6. (Pre-event) Life expectancy > 30 days.

排除标准

  • Subjects presenting with any of the following will not be included in the study:
  • 1. Severe immunosuppression (HIV infection, chemotherapy).
  • 2. Active neoplastic disease.
  • 3. Obstruction pneumonia (e.g. from lung cancer).
  • 4. Aspiration pneumonia.
  • 5. Pneumonia that developed within 8 days after hospital discharge.
  • 6. Unable and/or unlikely to comprehend and/or follow the protocol.
  • 7. Pregnant and/or lactating women.

研究者

发起方
Medisch Centrum Alkmaar

相似试验