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临床试验/NCT05978466
NCT05978466招募中不适用

MANAGEment of Atrial Fibrillation Outcomes Registry (MANAGE-AF)

CorVita Science Foundation1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2017年12月22日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,000
试验地点
1
主要终点
Number of participants who had thrombo-embolic event

研究概览

简要总结

The purpose of this research is to learn more about the normal care of patients with a new or pre-existing diagnosis of atrial fibrillation (AF). These abnormal and irregular heartbeats place patients at increased risk of developing clots in their bloodstream that could potentially lead to stroke. Normal care is designed to help prevent this from happening and to lessen or eliminate the symptoms patients may have. There are many different types of AF as well as numerous ways in which a variety of patients are treated. The investigators are interested in gathering more information to better keep track of patient treatment patterns (trends) that may differ from physician to physician, hospital to hospital, medication to medication, patient to patient and if necessary, procedure to procedure.

详细描述

The objective of this research is to establish a contemporary and simple to construct AF management registry that expands progressively over the continuum of care for each individual patient. The registry will be used to determine the course and progression of AF management in preventing thrombo-embolic events using rhythm and rate control interventions.

Primary endpoints:

  1. Atrial fibrillation natural history
  2. Thrombo-embolic event
  3. Death

Secondary endpoints:

  1. Bleeding
  2. Pro-arrhythmia
  3. Patient adherence
  4. Treatment complication

研究设计

研究类型
Observational
观察模型
Case Only
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

  • Diagnosis of valvular or non valvular atrial fibrillation
  • ECG documented atrial fibrillation A. 12 lead B. Rhythm strip C. Event monitor D. Holter Monitor E. Implantable loop recorder

排除标准

  • Age below 18 years.
  • Clinical evidence that death within 6 months is possible
  • Inability to consent to the research or sign a consent form
  • Inability to follow up at the research clinic at least annually for continuity of AF care and management

结局指标

主要结局

Number of participants who had thrombo-embolic event

时间窗: From enrollment to 10- year study completion

All strokes, transient ischemic and systemic thrombo-embolic events

Recurrence of Atrial fibrillation

时间窗: From enrollment to 10- year study completion

The natural progression of the condition will be assessed per medical record review

Mortality

时间窗: From enrollment to 10- year study completion

All cause death will be noted

次要结局

  • Number of participants who have experienced bleeding(From enrollment to 10- year study completion)
  • Number of patients who have had pro-arrhythmia events(From enrollment to 10- year study completion)
  • Number of patients who have had patient adherence events(From enrollment to 10- year study completion)
  • Treatment complication(From enrollment to 10- year study completion)

研究者

发起方
CorVita Science Foundation
申办方类型
Other
责任方
Sponsor

研究点 (1)

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