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临床试验/NCT03742180
NCT03742180撤回不适用

A Prospective Randomized Trial of Sublingual Ketorolac Compared to Intranasal Dexmedetomidine for Postoperative Analgesia in Pediatric Patients Undergoing Bilateral Myringotomy

Mansoura University1 个研究点 分布在 1 个国家开始时间: 2018年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
duration of analgesia

研究概览

简要总结

The investigators aim to compare intranasal dexmedetomidine in a dose of 1ug.kg-1 with sublingual ketorolac in a dose of 1mg.kg-1 on postoperative behaviour in those children undergoing BMT during their PACU stay

详细描述

Data were analyzed through SPSS (Statistical Package for Social Sciences), Program version 22. Distribution of data was first tested by Shapiro test. Data were presented as the mean and standard deviation (SD), median and range or numbers and percentages. For normally distributed data, an unpaired t-test was used to compare between mean values of both groups. For pain and sedation scores, Mann Whitney U test was used. Fisher's exact test was used for comparison of categorical data. The P value ≤ 0.05 was considered as the level of statistical significance.

A prior G power analysis was done. Using the results obtained from previous studies (14- 18) and assuming an alpha error of 0.05 and beta error 0f 0.2 (power of the study 80 %), a sample size of 60 patients per group was calculated. A drop out 10% of cases is expected, so; 33 cases per group will be required

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
2 Years 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • ASA physical status I- II.

排除标准

  • History of ketamine
  • History of NSAID
  • History of allergies
  • Any bleeding disorders
  • History of GIT bleeding
  • Those who will undergo other procedures in addition to bilateral myringotomy

研究组 & 干预措施

intranasal dexmedetomidine

Experimental

this group is planned for intranasal dexmedetomidine

干预措施: intranasal dexmedetomidine (Drug)

sublingual ketorolac

Active Comparator

this group is planned for sublingual ketorolac

干预措施: sublingual ketorolac (Drug)

结局指标

主要结局

duration of analgesia

时间窗: time from administering the study solution till the time for the first rescue analgesic] during first 24 hours

The duration of analgesia,define as the time to the first demand for rescue analgesic

次要结局

  • Nausea and vomiting(For 24 hours after surgery)
  • Heart rate(for 2 hours after the start of surgery)
  • Number of patients received rescue analgesics(For 24 hours after surgery)
  • Degree of sedation(For 24 hours after surgery)
  • Postoperative pain score(For 24 hours after surgery)
  • systolic blood pressure(for 2 hours after the start of surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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