跳至主要内容
临床试验/CTRI/2024/09/074208
CTRI/2024/09/074208尚未招募不适用

Comparison of two different dosages of premedication with dexmedetomidine to prevent adverse respiratory events after removal of supraglottic airway devices in paediatric patients.A prospective randomized study

DR ANKITA ASHISH1 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2024年9月25日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
130
试验地点
1
主要终点
To see occurence of any one of respiratory events like coughing,bronchospasm,LMA biting.

研究概览

简要总结

To study the  Effects of two different  doses of dexmedetomidine in  paediatric age group and see the primary adverse respiratory events like coughing,LMA  biting,   bronchospasm,airway obstruction, and study secondary outcome like emergence agitation,post operative nausea and vomiting, after removal of supraglottic airway devices.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
2.00 Year(s) 至 10.00 Year(s)(—)
性别
All

入选标准

  • 1.Parenteral consent.
  • 2.Patients of ASA grade 1&
  • 3.Patients scheduled for surgeries of less than 2 hours.

排除标准

  • 1.History of congenital heart disease,neurological disease and asthma.
  • 2.Patients with hiatal hernia,major abdominal or thoracic surgery.
  • 3.Patients with full stomach.
  • 4.Difficult airway or facial anomaly.

结局指标

主要结局

To see occurence of any one of respiratory events like coughing,bronchospasm,LMA biting.

时间窗: Baseline

次要结局

  • To see emergence agitation, postoperative nausea & vomiting.(Baseline)

研究者

发起方
DR ANKITA ASHISH
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

DR ANKITA ASHISH

Indira Gandhi Institute Of Medical Sciences

研究点 (1)

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