跳至主要内容
临床试验/NL-OMON44377
NL-OMON44377已完成不适用

Perioperative Management of Patients who are Receiving a Novel Oral Anticoagulant (Dabigatran, Rivaroxaban or Apixaban) and Require an Elective Surgery or Medical Procedure: A Prospective Cohort Study (PAUSE)* - PAUSE study

Academisch Medisch Centrum0 个研究点目标入组 20 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - age > 18 years
  • - receiving a NOAC (dabigatran or rivaroxaban or apixaban) for stroke prevention for Atrial Fibrillation (SPAF)
  • - ability to adhere to the NOAC discontinuation protocol
  • - patient will be undergoing any elective surgical procedure or intervention

排除标准

  • - CrCl <30 mL/min for dabigatran- and rivaroxaban-treated patients (<25 mL/min for apixaban-treated patients) as estimated by Cockroft-Gault formula
  • - Cognitive impairment or psychiatric illness that precludes collection of follow-up data
  • - Inability or unwillingness to provide informed consent
  • - Previous participation in this study having had a surgery/procedure performed

研究者

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