EUCTR2006-002098-30-NL进行中(未招募)不适用
Efficacy of Inhaled RhDNase in Mechanically Ventilated Pediatric Patients with an Atelectasis - RhDNase in ventilated pediatric patients
Erasmus Medical Centre Rotterdam0 个研究点目标入组 80 人开始时间: 2006年6月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 80
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
- •1. Age 0-18 years
- •2. Mechanical ventilation
- •3. Presence of an atelectasis on a chest radiograph (CXR)
- •4. First dose of study medication can be administered within 12 hours after an atelectasis has been diagnosed.
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Children with neuromuscular disorders and impaired ability to cough; cardiomyopathy; or cystic fibrosis.
- •2. Post-gestational age < 32 weeks
- •3. Mechanical ventilation during muscle paralysis
- •4. Atelectasis due to a bronchoscopically diagnosed:
- •- foreign body aspiration
- •- tracheal or bronchial compression by lymph nodes or vessels
- •5. RhDNase treatment in the previous 48 hours.
- •6. Clinical condition or ventilator settings that are not compatible with nebulizing medication (according to the responsible physician)
- •7. Presence of a pneumothorax
研究者
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