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临床试验/CTRI/2017/07/008995
CTRI/2017/07/008995已完成3 期

â??Clinical Profile of Hepatic Encephalopathy and comparison of Polyethylene Glycol (PEG) and Lactulose in the treatment of Overt Hepatic Encephalopathyâ?? - HELP-II

Institute of Medical Sciences0 个研究点目标入组 57 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
57

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. All patients diagnosed with Hepatic Encephalopathy presenting to the inpatient care at the department of Gastroenterology, IMS, BHU
  • 2. Age 18 to 80 years
  • 3. Diagnosis of Chronic Liver Disease from any cause
  • 4. The availability of a Legally Authorized Representative for interview and consent

排除标准

  • 1.Patients with Hepatic Encephalopathy
  • Grade I and Grade IV.
  • 2.Acute Liver failure
  • 3.More than 1 dose of lactulose before
  • 4.No Legally Authorized Representative to
  • give consent/ Refusal of consent
  • 5.Previously recruited in the present
  • 6.Serum Creatinine more than 2.5 mg /dl
  • 7.Treated with Vasopressors
  • 8.Pregnancy

研究者

发起方
Institute of Medical Sciences

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