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临床试验/NCT01742871
NCT01742871Unknown不适用

Nutritional Status of Patients Victims of Haemorragic Accidents With Antivitamins K

University Hospital, Clermont-Ferrand1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2012年8月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
300
试验地点
1
主要终点
Denutrition diagnosis

研究概览

简要总结

Bleeding under vitamin K antagonists are a major iatrogenic causes of hospitalization, subject to a fatal outcome in more than one third of cases, mortality is particularly high in cases of serious bleeding, including intracerebral hemorrhage. If the INR measured in these patients are often away from the higher value of the target range, a significant proportion of bleeding were observed for INR between 2 and 3. The study captures the components of the nutritional status of patients on oral anticoagulants, including any micronutrient deficiencies, to determine whether nutritional status is an independent risk factor for bleeding

详细描述

Be included in this study patients under anti-vitamin K supported or followed the emergency department Adults.

The inclusion visit will be conducted in the emergency department Adults Clermont-Ferrand by an emergency physician or investigator or co-investigator. The protocol will be explained to patients in detail, the information document and consent will be issued for playback, then they will be asked to sign the consent form and participation agreement.

Case-control study: patients under oral anticoagulant with severe hemorrhagic accident compared with patients without hemorrhagic accident. Cases will be matched to controls based on age, sex, and the value of the INR.

Patients will be divided into two groups:

  • Group 1: cases Patient under anti-vitamin K with a serious bleeding event that required treatment in the emergency Adults. Is considered serious accident requiring the use of a reversion by PPSB (Kaskadil ®).
  • Group 2: contols Patient under anti-vitamin K with no haemorrhagic manifestations admitted for another reason to Emergency Adults

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients, male or female, aged over 18, under oral anticoagulant therapy with antivitamins K.
  • INR greater than 1.5, in the therapeutic range or overdose
  • Patient have read, understood and signed the consent form or inclusion emergency consent of the person with confidence
  • Case-control study: patients under oral anticoagulant with severe hemorrhagic accident compared with patients without hemorrhagic accident. Cases will be matched to controls based on age, sex, and the value of INR :
  • Patients victims of serious hemorrhagic accident on VKAs, supported emergency Adults.
  • Will be considered severe hemorrhagic stroke, accidents requiring the use of a reversion by PPSB (Kaskadil ®)
  • Patients on VKAs supported the Emergency Adults for a reason other than bleeding.

排除标准

  • underage patients
  • Patients who have not read or understood nor signed the consent form or refusal of the reference person.
  • pregnant women
  • Patients with a pacemaker and / or implantable defibrillator
  • Patients with mechanical valve

结局指标

主要结局

Denutrition diagnosis

时间窗: at day 1

次要结局

  • vitamin C blood level(at day 1)
  • vitamin B1 blood level(at day 1)
  • Cupper blood level(at day 1)
  • Zinc blood level(at day 1)
  • PINI (pronostic inflammatory and nutritional index)(at day 1)
  • NRI (nutritional risk index)(at day 1)
  • The outpatient bleeding risk index(at day 1)
  • Stiffness index(at day 1)
  • Rumpel-Leede test(at day 1)

研究者

发起方
University Hospital, Clermont-Ferrand
申办方类型
Other
责任方
Sponsor

研究点 (1)

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