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临床试验/SLCTR/2014/023
SLCTR/2014/023招募中2 期

Effect of Rupatadine compared to placebo in the reducing complications of acute dengue infection

Centre for Dengue Research, University of Sri Jayawardenapura0 个研究点目标入组 240 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
240

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. Confirmed dengue infection (positive dengue NS1 antigen detection test or presence of dengue specific antibodies)
  • 2. Informed written consent
  • 3. Age: between 18-60 years
  • 4. Duration of illness: less than 5 days
  • 5. No evidence of vascular leak.

排除标准

  • 1. Pregnancy
  • 2. Known allergies to antihistamines
  • 3. Individuals who are homeless
  • 4. Dependency on alcohol or abuse drugs
  • 5. Hepatic impairment defined as: no previously known liver disease, prolonged prothromin time of 4-6 seconds or more, INR of >1.5
  • 6. Renal impairment defined as: hypertension and diabetes, GFR <60 ml/min per 1.73 m2, urinary albumin-to-creatinine ratio >30 mg/g , hereditary kidney disease, recurrent or extensive nephrolithiasis, urinary red cell casts, red blood cell count >20 per high power field, Consistent albuminuria

研究者

发起方
Centre for Dengue Research, University of Sri Jayawardenapura

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