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临床试验/EUCTR2017-003643-38-FR
EUCTR2017-003643-38-FR进行中(未招募)1 期

INTRANASAL KETAMINE IN THE REDUCTION OF THE ISOLATED FRACTURES OF THE HIGHER MEMBER OF THE CHILD TO PEDIATRIC EMERGENCIES - KETA PED

Fondation Lenval - Hôpitaux Pédiatriques de Nice CHU-LENVA0 个研究点目标入组 60 人开始时间: 2018年1月16日最近更新:
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
60

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

  • -Male or Female Children
  • -Aged 4 to 17 years old
  • - Presenting a fracture isolated from the distal end of the upper limb with closed focus, requiring a reduction
  • - Fracture dating from <72h
  • - stable hemodynamics
  • - Affiliation to a social security scheme
  • - Signature of the authorization documents of the 2 parents or the representative of the parental authority for the participation of the child in the study
  • - Signature of informed consent for children over 15 years of age
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 60
  • 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

  • -Known hypersensitivity to ketamine
  • -History of epilepsy or known psychiatric illness
  • -Any child with a developing respiratory disease (asthma, laryngitis, tracheitis)
  • -Any child who has received an analgesic of level 2 or 3 in the 3 hours preceding the treatment in pediatric emergencies
  • -High Blood Pressure
  • -Severe Heart Failure
  • -polytrauma
  • -Open fracture
  • -Proven pregnancy
  • - Any child requiring pure oxygen ventilation.
  • - Nitrous oxide should not be used in situations at risk of accumulation in cavities and when its expansion could be dangerous, such as cranial trauma with alteration of the state of consciousness, maxillofacial trauma, pneumothorax, gas embolism , bullous emphysema, sinus or middle ear surgery, internal ear surgery, severe abdominal distension (eg, bowel occlusion)
  • - A child who has recently received an ophthalmic gas (SF6, C3F8, C2F6) used in ocular surgery as long as a gas bubble persists inside the eye and at a minimum for a period of 3 months. Severe post-operative complications may occur in relation to increased intraocular pressure

研究者

发起方
Fondation Lenval - Hôpitaux Pédiatriques de Nice CHU-LENVA

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