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临床试验/NCT06144398
NCT06144398已完成不适用

Single Use Versus Standard Flexible Bronchoscopes in Interventional Pulmonary Procedures: an Open Label Randomized Controlled Trial

Clinical Hospital Centre Zagreb2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年11月27日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
20
试验地点
2
主要终点
Overall performance

研究概览

简要总结

Single Use Flexible bronchoscopes have gained popularity in recent years and are becoming technologically more advanced. They are widely accepted and used in everyday practice for simple procedures. The aim of this study is to evaluate single use flexible bronchoscopes in more advanced settings, such as interventional pulmonary procedures.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients requiring an interventional pulmonary procedure during the study period
  • Signed informed consent

排除标准

  • Any patient with a contraindication for rigid and/or flexible bronchoscopy
  • Coagulopathy (PV INR > 1.3)
  • Thrombocytopenia (<50x10*9 or anemia (Hgb <80 g/L)
  • DOAC, LMWH or antiplatelet drug therapy
  • Thrombophilia, history of pulmonary embolism or deep vein thrombosis
  • Contraindication for endobronchial application of adrenaline
  • Uncontrolled coronary artery disease, cerebrovascular disease or arrhythmia
  • Uncontrolled pulmonary hypertension
  • Cardiovascular decompensation
  • Severe hypoxia (PaO2 <60mmHg, SaO2 <90% with an FiO2 >=60%)
  • Cervical spine instability

结局指标

主要结局

Overall performance

时间窗: through study completion, an average of 12 months

Overall performance of the bronchoscope as graded by the operator (on a scale from 1 to 10; 1 worse, 10 best performance)

次要结局

  • Functionality, handle and interface(through study completion, an average of 12 months)
  • Suction(through study completion, an average of 12 months)
  • Image quality(through study completion, an average of 12 months)
  • Bleeding control(through study completion, an average of 12 months)
  • Compatibility(through study completion, an average of 12 months)

研究者

发起方
Clinical Hospital Centre Zagreb
申办方类型
Other
责任方
Principal Investigator
主要研究者

Goran Glodić

MD, Principal Investigator

Clinical Hospital Centre Zagreb

研究点 (2)

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