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临床试验/EUCTR2012-002792-34-GB
EUCTR2012-002792-34-GB进行中(未招募)1 期

Phenotyping bronchiectasis based on aetiology, exacerbation characteristics and response to erythromycin. - Phenotyping bronchiectasis over 2 years including a macrolide trial

niversity Hospitals Leicester NHS Trust0 个研究点目标入组 90 人开始时间: 2014年3月13日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Group 1 - 40 participants over 2 years including the intervention
  • - Patients who have clinical symptoms suggestive of bronchiectasis confirmed by CT scan.
  • - Aged 18-100.
  • - Ability to give valid consent.
  • - Willingness to attend the hospital every 3 months for 2 years.
  • Group 2 - 50 participants for baseline visit only
  • - Patients who have clinical symptoms suggestive of bronchiectasis confirmed by CT scan.
  • - Aged 18-100.
  • - Ability to give valid consent.
  • - Willingness to attend the hospital for a one off visit.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 15
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 25

排除标准

  • Group 1 - 40 participants over 2 years including the intervention
  • - Active TB.
  • - Patients under 18 and over 100.
  • - Patients who are too unwell to attend visits.
  • - Patients with known cystic fibrosis.
  • - Patients with traction bronchiectasis secondary to fibrosis.
  • - Patients who are unable to consent.
  • - Patients already on long term antibiotics.
  • - Patients with macrolide allergy / severe intolerance / prolonged QT interval.
  • - Patients taking medication with a known interaction with erythromycin where the use is contraindicated, with the exception of simvastatin.
  • Group 2 - 50 participants for baseline visit only
  • - Active TB.
  • - Patients under 18 and over 100.
  • - Patients who are too unwell to attend visits.
  • - Patients with known cystic fibrosis.
  • - Patients with traction bronchiectasis secondary to fibrosis.
  • - Patients who are unable to consent.

研究者

发起方
niversity Hospitals Leicester NHS Trust

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