EUCTR2010-022863-36-ES进行中（未招募）不适用
Phase IV, randomized and controlled study about efficacy an safety of theuse of continuous pressure airway CPAP Bussignac in the immediatepostoperative period of patients undergoing lung resection surgery, asprophylaxis of postoperative complications
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
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)Being over 18 and ethically competent.
- •2)Undergo any thoracic surgery including resection of lung parenchyma and carriers of thoracic epidural or paravertebral catheter for perioperative thoracic analgesia.
- •3)To have given written consent to enter this study.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 230
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 230
排除标准
- •1)Patients who have not been extubated in the first 4 h post surgery.
- •2)Patients with suspected bronchopleural fistula at PCU admission .
- •3)Patients with facial problems or patients with a history of intolerance
- •to CPAP masks.
- •4)Having significant bullous emphysema.
- •5)Patients having Obstructive apnea syndrome and have been
- •recomended of any kind of noninvasive ventilation.
- •6)Patients who have consumed at least one month before surgery
- •potential immunosuppressive drugs (except corticosteroids administered
- •by inhalation).
研究者
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