跳至主要内容
临床试验/EUCTR2009-017153-35-IT
EUCTR2009-017153-35-IT进行中(未招募)不适用

An international, multi-center, randomized, controlled trial evaluating the effect of xenon on postoperative delirium in elderly patients undergoing hip fracture surgery. - Hip fracture surgery in elderly patients

AIR LIQUIDE SANTE` INTERNATIONA0 个研究点目标入组 256 人开始时间: 2010年8月23日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
256

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

  • - Elderly patient (75 years and older). - Patients with planned hip fracture surgery within 48 hours after the hip fracture. - Patient willing and able to complete the requirements of this study including the signature of the written informed consent.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • 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) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Patient suffering of multiple fractures, pelvic fractures proximal, pathological fractures, femur fractures (ie fracture of the middle and distal femur). - Disabling neuropsychiatric disorders (severe dementia, Alzheimer’s disease, schizophrenia, depression). - Brain trauma within 12 months prior to selection, history of stroke with residuals. - Patient suffering from delirium (CAM diagnosis) at selection. - Patients who cannot complete the pre-operative mental tests of this current clinical trial - Patients with Mini-Mental State Examination (MMSE) score < 24 at selection. - Contra-indication (serious illness or medical conditions) for general anaesthesia . - Known allergy or hypersensitivity to any drugs administered during the current clinical trial. - Previous participation in this current clinical trial. - Participation in another clinical trial within 4 weeks prior to selection. - History of alcohol or drug abuse or psychiatric disorders which would impair the understanding of the necessary information or render medically or legally unable to give written informed consent.

研究者

发起方
AIR LIQUIDE SANTE` INTERNATIONA

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