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临床试验/CTRI/2026/01/102255
CTRI/2026/01/102255尚未招募不适用

Comparison of continuous infusion of dexmedetomidine vs remifentanyl for conscious sedation in patients undergoing transcatheter aortic valve replacement -a single blinded randomized control trial

Medanta the medicity1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2026年2月7日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
80
试验地点
1

研究概览

简要总结

patients will be grouped into two groups.Group D will receive dexmeditomidine and group R will receive remifentanyl and comparison of sedative effects of both these drugs on sedation will be done in patients undergoing transcatheter aortic valve replacement.Other parameters like ABG and hemodynamics will be recorded.postoperative delirium,length of ICU stay,postoperative nausea and vomiting,patient and cardiologist satisfaction and BIS values will also be recorded.And we expect remifentanyl to a a better hemodynamic and sedative effects than dexmedetomidine with lesser or no adverse events.

研究设计

研究类型
Observational

入排标准

年龄范围
60.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • patients more than 60 years with severe aortic stenosis with symptoms such as chest pain,palpitation and with preserved systolic funtion.

排除标准

  • recent MI or stroke within last 6 months,CAD,patients not giving consent,EF less than 60 percent.

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Christy Pius Kaliyadan

Medanta the medicity

研究点 (1)

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