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临床试验/EUCTR2015-002175-24-FR
EUCTR2015-002175-24-FR进行中(未招募)不适用

Effect of the exacyl on perioperative bleeding during surgery of orthognatism of the upper maxillary - LEFORT1/EXACY

Centre Hospitalier Régional et Universitaire de Lille0 个研究点开始时间: 2015年8月5日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

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

  • -Underage from = 12 to 17 years old or an Adult from = 18 years old
  • -Patient that must be operated for an osteotomy of the upper maxillary isolated or associated with an osteotomy of the lower maxillary and / or with a génioplastie within the framework of a surgery of orthognatism
  • -Hb = 12g / dL on the preoperative screening
  • -Patient ASA (American Society of Anesthesiologists) 1 or 2
  • -Patient non pregnant
  • -Be a person covered by Social Security
  • -Signed Consent
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 189
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 21
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patient presenting disorders of the hemostasis
  • Patient under anticoagulation treatment or antiagrégant
  • Patient requiring a treatment anticoagulation in operating comment
  • Patient presenting a contraindication to the EXACYL (renal insufficiency engraves(burns), histories of convulsions, histories of accidents thrombo-embolics venous or arterial)
  • Surgery recognized preoperative as particularly complicated by the surgeons
  • Pregnant Women
  • Nursing mothers
  • People in emergency situation
  • Incapable people and specially protected mentioned in the article L 1121-5 to L1121-8 are not included in the study

研究者

发起方
Centre Hospitalier Régional et Universitaire de Lille

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