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临床试验/PACTR201712002863123
PACTR201712002863123尚未招募未知

Comparative study of multiple doses regimen of Dexmedetomidine used for moderate sedation facilitating intubation condition during nasotracheal fiberoptic laryngoscope in awake patients. Randomized prospective study.

Faculty of Medicine, Aswan University0 个研究点目标入组 40 人开始时间: 2017年12月12日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
发起方
入组人数
40

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
30 Year(s) 至 70 Year(s)(—)
性别
All

入选标准

  • patients with ASA patients status I and II

排除标准

  • Patients with obesity more than 30% above the ideal body weight, patients refusal,gastroesophageal reflux, uncontrolled blood pressure, ischemic heart diseases, diabetic, asthmatic, severe bradycardia or any type of A-V block on ECG,coagulapthy, hepatic, renal dysfunction thrombocytopenia, hyperactive air way diseases, , history of drug maluse,and a long term use of benzodiazepines or antidepressant drugs, any neurological disorders or mental retardation, pregnancy, nasal polyp, history of allergy to any used medication, any apparent airway abnormalities with mallampati score ¿ III(7), thyromental distance ¿ 6 centimeters and history of laryngeal or pharyngeal surgeries all were excluded from our study.

研究者

发起方
Faculty of Medicine, Aswan University

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