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临床试验/EUCTR2018-000196-32-ES
EUCTR2018-000196-32-ES进行中(未招募)1 期

PILOT STUDY ON THE USE OF HYDROCORTISONE, VITAMIN C AND THYAMINE IN PATIENT WITH SEPSIS AND SEPTIC SHOCK.

HU DE GIRONA DR JOSEP TRUETA0 个研究点目标入组 40 人开始时间: 2018年10月1日最近更新:
适应症
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
40

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

  • * Patients> 18 years of age with diagnosis of septic shock and multiple organ failure admitted to our Unit
  • * Admission in ICU once diagnosed of sepsis and / or septic shock. The first 24 hours after admission to the ICU will be established as the inclusion limit.
  • * Signed Informed consent form
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 20
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • * Patients under 18 years of age
  • * Pregnancy
  • * Coexistence of other types of shock at the time of admission
  • * Limitation of therapeutic effort or ICT (Conditioned Intensive Therapy) to admission to the ICU. It refers to patients in whom prior to admission to the ICU it has been decided not to perform any or some of the usual treatment measures of sepsis, or in which a time limit is established in which, in case of non-response, they would withdraw intensive measures. This limitation will be indicated by your treating doctor and if it exists, the patient would be excluded from the study.
  • * Patient with a history of previous intake of ascorbic acid, thiamin or corticosteroids in the month prior to admission to the ICU
  • * Patients considered immunodeficient (more than 10 mg of prednisone or its equivalent per day in the last 2 weeks, immunosuppressive therapy or diagnosis of acquired immunodeficiency syndrome).

研究者

发起方
HU DE GIRONA DR JOSEP TRUETA

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