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临床试验/CTRI/2013/02/003438
CTRI/2013/02/003438已完成Phase 3 4

The Effect of Intranasal Dexmedetomidine or Oral Midazolam Premedication on the Minimum Alveolar Concentration of Sevoflurane for the Insertion of Laryngeal Mask Airway in children. A comparative study

Post Graduate Institute of Medical Education and Research1 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2012年1月23日最近更新:

试验速览

阶段
Phase 3 4
状态
已完成
发起方
入组人数
56
试验地点
1
主要终点
To determine and compare the EC50 of sevoflurane for LMA insertion in children in all the three groups

研究概览

简要总结

The study was planned to evaluate andcompare the effect of   intranasal dexmedetomidine or oral midazolam onthe EC50 requirement of sevoflurane for LMA insertion in childrencompared to placebo.  56 ASA 1children (1-6yrs) scheduled for general anaesthesia with LMA were randomly allocated tothree groups: group M received 0.5 mg/Kg oral midazolam and intranasal saline, groupD received 2µg/Kg  intranasaldexmedetomidine along with oral honey, and  group P received oral honey and intranasalsaline 30min before procedure. Anesthesia was induced with sevoflurane.Apredetermined target end-tidal sevoflurae concentration (starting at 2%) was maintained for 10 min using Dixon’sup-down method and the laryngeal mask airway was inserted without neuromuscularblockade. The target end-tidal concentration in the next patient was increasedor decreased by 0.2% depending upon the response of the previous patient.Insertion of the laryngeal mask airway without coughing, clenching, biting,movement or any adverse airway event during or within 1 min after insertion wasconsidered to be successful.in case of success the ET sevoflurane concentartion was decreased by 0.2% otherwise it was increased by 0.2%. All responses to an LMA insertion wereassessed with the LMA insertion score.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded

入排标准

年龄范围
1.00 Year(s) 至 6.00 Year(s)(—)
性别
All

入选标准

  • ASA 1 and 2 patients of either gender of the age 1- 6 years undergoing any short elective surgical procedure under general anaesthesia which can be performed with LMA insertion.

排除标准

  • airway malformations, clinical evidence of patients with difficult airway, asthma or any sign of upper respiratory tract infection, G6PD deficiency, organ dysfunction , allergy or hypersensitive reaction to dexmedetomidine , known cardiac arrhythmia or congenital heart disease, mentally disabled , known case of autism or developmental pervasive disorder or failure to insert LMA.

结局指标

主要结局

To determine and compare the EC50 of sevoflurane for LMA insertion in children in all the three groups

时间窗: At or one minute after LMA insertion

次要结局

  • Ramsay Sedation Score, parental separation score, induction score success rate, and the incidence of adverse events(Ramsay sedation score at baseline, 15 and 30 minutes after premedication, parental separation score at taking the child in the OT and induction score at placing the face mask, adverse events at or one minute after LMA insretion)

研究者

发起方
Post Graduate Institute of Medical Education and Research
申办方类型
Research institution and hospital

研究点 (1)

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