EUCTR2017-000057-40-SE进行中(未招募)1 期
A prospective randomized double-blind studyIntranasal dexmedetomidine versus intranasal S-ketamine for children age1 – 3 years for procedural sedation and analgesia in pediatric emergencydepartment.
Karolinska University Hospital0 个研究点目标入组 30 人开始时间: 2017年1月13日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Children at the age of 1 - 3 years who present to the emergency
- •- A laceration in need of suturing or burn less than 4% of body surface
- •- Weight 10 – 15 kg
- •- Previously healthy
- •- Swedish speaking
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 52
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •ASA classification = III (see Supplement 12)
- •Current respiratory tract infection
- •Impaired level of consciousness
- •Hypersensitivity for dexmedetomidine or S-ketamine.
- •Further contraindications named in the product resume for the trial
- •medicines would categorize the patient as ASA III and therefore not
- •suitable for this trial.
- •- advanced heart block (grade 2 or 3) unless paced
- •- uncontrolled hypotension
- •- acute cerebrovascular conditions.
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