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临床试验/ACTRN12620000830998
ACTRN12620000830998终止未知

Immunogenicity of the influenza vaccination in patients with chronic obstructive pulmonary disease (COPD).

Princess Alexandra Hospital0 个研究点目标入组 171 人开始时间: 2020年8月21日最近更新:
适应症

试验速览

阶段
未知
状态
终止
入组人数
171

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
50 Years 至 o limit(—)
性别
All

入选标准

  • Mild to very Severe COPD with a post bronchiodilater FEV1 less than 80% predicted FEV1 /FVC ratio less than 0.7. COPD patients will be stable with no COPD exacerbations or respiratory infections within the last 4 weeks.
  • Healthy controls no prior or current symptoms of lung disease, MRC dyspnoea scale less than 2 and normal spirometry. And normal spirometry with an FEV1 and FVC within normal range.

排除标准

  • Invasive malignancy within the last 2 years.
  • Renal impairment (eGFR less than 40ml/min).
  • Acute febrile illness with fever greater than 38.5 dC.
  • Hypersensitivity to egg protein.
  • Use of oral Prednisolone (or equivalent) greater than or equal to 10mg per day.
  • Use of other systemic immunosuppressive therapy.
  • Anaphylaxis following a previous dose of influenza vaccine.
  • Anaphylaxis following a vaccine component (including eggs).
  • History of Guilliane Barre within 6 weeks of a previous influenza vaccination
  • Cardiac disease, diabetes mellitus and superficial non- melanoma skin cancers WILL NOT be exclusion criteria provided these are stable and well controlled in the opinion of the investigator.

研究者

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