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
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