CTIS2023-506803-25-01进行中(未招募)1 期
AntaMIn - Pain reduction for limb injuries in pediatric emergency departments: A Randomised Clinical Trial comparing intranasal Fentanyl or intranasal Ketamine to oral morphine - APHP211044
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 300
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 0 至 17(—)
- 性别
- All
入选标准
- •1)Child aged 2 years to 17 years and 11 months, With 10 kg = Weight = 100 kg, Presenting to ED with a traumatic pain and suspected fracture(s) based on an acute deformity AND experiencing pain and / or functional impotence in the injured limb(s), Within the first 12 hours after the injury, VAS pain score at ED arrival = 60/100 (if child = 7) or Evendol pain score at ED arrival = 7/15 (if child <7 years), Affiliated to health insurance, At least one signed parental informed consent
排除标准
- •Received narcotic pain medication prior to arrival, Contraindication to fentanyl or ketamine, mentioned in SmPC, GCS <15, Evidence of significant femur, head, chest, abdominal, or spine injury, Open fracture, Nasal trauma or complete nasal obstruction, Active epistaxis, Nasal or sinus surgery within 6 months before inclusion, History of high blood pressure, known coronary artery disease, congestive heart failure, acute glaucoma, increased intracranial pressure, , hepatocellular insufficiency, Active or history of psychiatric disorder, Known pregnancy or suspicion of being pregnant, Breastfeeding, Non-French speaking parent and / or child., Participation to another interventional clinical research, Contraindication to morphine, mentioned in SmPC, Hypersensitivity to ketamine or fentanyl or to excipients (sodium chloride, sodium hydroxide), or to other opioids.
研究者
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