CTRI/2023/06/054292已完成Unknown
A Bispectral index guided comparison of Propofol-Fentanyl and Propofol-Dexmedetomidine combinations for intravenous sedation in Endoscopic Retrograde Cholangiopancreatography (ERCP)
WASIM WAHID0 个研究点目标入组 81 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 81
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Patient undergoing ERCP under iv sedation
- •1)ASA physical status I,II and III
- •2)Body weight :40 to 70 kg
排除标准
- •1)Allergy or history of adverse reaction to Propofol, Dexmedetomidine or Fentanyl
- •2)Pregnancy or lactation
- •3)Anticipated difficult airway
- •4)Patients with chronic kidney disease, neurological deficit, pre-existing delirium/cognitive dysfunction
- •5)Evidence of hepatic encephalopathy or ascites
- •6)Hyponatremia ( <120 meq/l) and hypo or hyperkalemia ( <3meq/l and >5.5 meq/l)
- •7)Patient refusal
- •8)Patients with comorbidities like uncontrolled hypertension, hypotension, uncontrolled diabetes mellitus, congestive cardiac failure, and low cardiac output disorders or arrhythmias.
研究者
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