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临床试验/NCT03871283
NCT03871283已完成不适用

Anticoagulation and Antiplatelet Management During Perioperative Period : a Daily Practice Cohort Prospective Study

Erasme University Hospital1 个研究点 分布在 1 个国家目标入组 2,400 人开始时间: 2019年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
2,400
试验地点
1
主要终点
Ratio of well treated patient

研究概览

简要总结

the investigators hypothesize that patients do not understand these therapies, and that they are poorly undertaken. In some cases, the anesthesiologist does not understand correctly the indication of the treatment due to lack of information and therefore does not know how to adapt it to the medical situation.

详细描述

the investigators hypothesize that patients do not understand these therapies, and that they are poorly undertaken. In some cases, the anesthesiologist does not understand correctly the indication of the treatment due to lack of information and therefore does not know how to adapt it to the medical situation.

the investigators want to investigate these transitions: how were they understood by patients, how were they performed, and how does this affect surgery, postoperative morbidity and mortality?

Anticoagulation for prevention of thromboembolic events will not be studied in this study.

The anesthesia team will not be particularly trained in anticoagulants and antiplatelets management to be close to actual care. In the Hospital the investigators have a guide written in 2013 in order to describe all the cases possible. The "control/ goal group" will be the patients who have undertaken strictly the protocol described for their cases in the guide.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients over 18 years old
  • Able to consent
  • Taking anticoagulants or antiplatelet drugs in the long term.

排除标准

  • Incapacitated adults
  • Minor patients

结局指标

主要结局

Ratio of well treated patient

时间窗: 30 days

Ratio of well treated patient

次要结局

  • bleeding consequence (volume in mL)(30 days)
  • Mortality Consequence(30 Days)
  • Blood Test Consequence(30 Days)
  • Morbidity(30 days)

研究者

发起方
Erasme University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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