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临床试验/CTRI/2024/04/065164
CTRI/2024/04/065164招募中不适用

A Study on 72 hour Ambulatory ECG monitoring in acute ischemic stroke

Department of General Medicine1 个研究点 分布在 1 个国家目标入组 166 人开始时间: 2024年5月1日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
166
试验地点
1
主要终点
The incidence of cardiac arrhythmias detected by ambulatory ECG monitoring in patients with acute ischemic stroke will be calculated

研究概览

简要总结

Patients who have suffered an acute ischemic stroke as per the inclusion and exclusion criteria are selected, and explained about the study and enrolled after taking informed consent from patient or patient caretakers.

Baseline investigations will be noted and those patients whose baseline ECG is not suggestive of atrial fibrillation and neuroimaging suggestive of acute ischemic stroke will be evaluated with 72 hours ambulatory ECG monitoring and report will be collected after cardiologist confirmation. Abnormal rhythms if present will be noted

Patients who are started on anti coagulation based on the ECG monitoring report will be noted

Data will be entered in the Microsoft excel sheet and will be analysed with appropriate statistical measures, and results will be arrived.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • All Patients who have suffered an acute ischemic stroke, and documented by CT/MRI, and undergoing 72 hour ambulatory ECG monitoring.
  • All patients who have suffered a transient ischemic attack (TIA).
  • All stroke patients whose baseline ECG is not showing atrial fibrillation.

排除标准

  • All Patients who have suffered an acute CVA due to hemorrhagic stroke.
  • All patients whose baseline ECG is suggestive of atrial fibrillation.
  • All patients whose age less than 18 years.
  • All Patients who are carrying a pacemaker with atrial lead.

结局指标

主要结局

The incidence of cardiac arrhythmias detected by ambulatory ECG monitoring in patients with acute ischemic stroke will be calculated

时间窗: Case control study for 2 years

The number of patients in whom anticoagulation is initiated based on the ECG monitoring report will be calculated

时间窗: Case control study for 2 years

次要结局

  • The detection of arrhythmias in the first 24 hours versus the next 48 hours will be compared(Case control study for 2 years)

研究者

发起方
Department of General Medicine
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

DR ARAVINDH SHIVA G

Kasturba Hospital Manipal

研究点 (1)

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