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临床试验/TCTR20230221003
TCTR20230221003已完成4 期

A Randomized Controlled Trial Comparing the Diagnostic Yield of using Rapid On-Site Cytology Evaluation (ROSE) and without using ROSE in Radial Probe Endobronchial Ultrasound (R-EBUS) Guided Sheath Transbronchial Lung Biopsy with Bronchial Brushing in Peripheral Pulmonary Lesions.

King Chulalongkorn Memorial hospital0 个研究点目标入组 68 人开始时间: 2023年2月21日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
68

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

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1. All patients over 18 years old
  • 2.All patients diagnosed with peripheral lung lesions or nodule size smaller than or equal to 3 centimeters from chest computed tomography.

排除标准

  • Patients who have bronchoscopy contraindications
  • -No consent for the procedure
  • -Patients do not cooperate during the procedure.
  • -Risk of hemorrhagic conditions such as Severe Thrombocytopenia (Platelet <20000) , Coagulopathy ( INR < 2) that have not been resolved.
  • -Severe or refractory hypoxia (SpO2 < 90%)
  • -Unstable Hemodynamic Status : BP <90/60, MAP < 65, HR < 50 or > 130, RR>30
  • -Myocardial Infarction within 4-6 weeks
  • -Patients who increased intracranial pressure
  • -Severe pulmonary arterial hypertension
  • -Other relative contraindication conditions depend on judgement of doctor, such as uremia and Superior Vena Cava Obstruction.

研究者

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