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临床试验/CTRI/2015/01/005465
CTRI/2015/01/005465招募中2 期

A comparative study of dexmedetomidine and propofol for sedation during endoscopic retrograde cholangiopancreatography(ERCP) in patients with impaired liver functionâ??

IDA NAWAZ0 个研究点目标入组 50 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
50

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

  • Patients undergoing elective ERCP with impaired liver function (i.e. raised serum bilirubin ,SGOT or SGPT levels)
  • Normal prothrombin time (PT) and international normalized ratio (INR)
  • ASA grade II.
  • Aged between 18 and 60 years.
  • Those who are willing to give written informed consent

排除标准

  • ASA grade III or more.
  • Patients with comorbid conditions such as HTN, DM or renal insufficiency.
  • Patients having difficulty in communication (due to language problem or deafness).
  • Patients with history of operative intervention in the past 72 hrs.
  • Patients with the known allergy to these drugs and with a history of sulphite ,egg or soyabean allergy
  • Pregnant patients.

研究者

发起方
IDA NAWAZ

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