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A Study on continuous monitoring of heart rhythm for 72 hours, in patients who have suffered a stroke, using a patch like device, to find out the occurence of abnormal heart rhythms in such patients.

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/04/065164
Enrollment
166
Registered
2024-04-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G40-G47- Episodic and paroxysmal disorders

Interventions

Intervention1: NIL: NIL Intervention2: NIL: NIL

Sponsors

Department of General Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

MeasureTime frame
The incidence of cardiac arrhythmias detected by ambulatory ECG monitoring in patients with acute ischemic stroke will be calculated The number of patients in whom anticoagulation is initiated based on the ECG monitoring report will be calculatedTimepoint: Case control study for 2 years—

Secondary

MeasureTime frame
The detection of arrhythmias in the first 24 hours versus the next 48 hours will be comparedTimepoint: Case control study for 2 years—

Countries

India

Contacts

Public ContactDR ARAVINDH SHIVA G

Kasturba Hospital Manipal

adharsha.gk@manipal.edu9591706468

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026