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临床试验/TCTR20200916008
TCTR20200916008招募中4 期

Effect of Continuous Positive Airway Pressure on Time to Resolution of Dengue-associated Pleural Effusion

Mahidol Oxford Research Unit0 个研究点目标入组 74 人开始时间: 2020年9月16日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
74

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
19 Years 至 100 Years(—)
性别
All

入选标准

  • 1.Age > 18 years;
  • 2.Dengue infection confirmed by either antigen detection e.g. PCR for RNA, NS1Ag or antibodies detection e.g. IgM ELISA, paired IgG ELISA methods;
  • 3.Newly detected pleural effusion of at least 2 centimeters detected by chest ultrasound at posterior part of right diaphragm in upright position in 24 to 48 hours after fever has disappeared.

排除标准

  • 1. An underlying disorder causative of pleural effusion e.g. tuberculous effusion, malignancy effusion, cirrhosis, heart failure, etc.
  • 2.Contraindication to CPAP, e.g., coma, shock or known intolerance for NIV/CPAP
  • 3.Pregnancy
  • 4.No informed consent
  • 5. Cannot communicate with Thai or English language

研究者

发起方
Mahidol Oxford Research Unit

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