CTRI/2023/10/058887尚未招募3 期
A randomized controlled, double blinded study to test the efficacy of Protective One Lung Ventilation Bundle in prevention of Post Operative Pulmonary Complications following elective major lung resection surgeries in a tertiary care cancer institute. - P-OLV
Tata Memorial Hospital Mumbai India0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1.Age between 18-80 years
- •2.Patients scheduled for open thoracic or video-assisted thoracoscopic or robot-assisted lung resection onco-surgery which would involve planned resection of at least one lobe of the lung.
- •3.The planned duration of surgery is more than 60 minutes.
排除标准
- •1.Patients with documented evidence of chronic obstructive pulmonary disease (COPD) GOLD grades III and IV, interstitial lung disease with a GAP index >4, documented bullae (occupying more than one-third of the hemithorax).
- •2.Patients with uncontrolled asthma
- •3.patients with heart failure New York Heart Association grade 3 and 4 or coronary heart disease, showing a positive stress test or inducible ischemia on stress echocardiography;
- •4.patients with previous lung surgery;
- •5.patients with at-rest documented mean pulmonary arterial pressure > 25 mmHg, or systolic pulmonary arterial pressure > 35 mmHg (as estimated by echocardiography);
- •6.patients with documented or suspected neuromuscular disease (e.g., thymoma, myasthenia, myopathies, muscular dystrophies);
- •7. patients who are planned for mechanical ventilation after surgery prior to anaesthesia induction;
- •8. Patients who are planned for bilateral procedures;
研究者
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