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.
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