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Magnesium Sulphate in patients with new onset atrial fibrillation

A Prospective Observational Study of Magnesium sulphate in Patients with New Onset Atrial Fibrillation - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/11/076176
Enrollment
79
Registered
2024-11-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: I489- Unspecified atrial fibrillation and atrial flutter

Interventions

Intervention1: Magnesium sulphate: Administration of Intravenous Injection of magnesium sulphate of 4500 mg standard dose in new onset atrial fibrillation Control Intervention1: NIL: NIL

Sponsors

Rishwanth Raja P M
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Age 18 years or more 2)New onset atrial fibrillation(within 48 hours) of presentation,persist for atleast 30mins,ventricular rate 120 beats per minute or more without evidence of volume depletion 3)Normal Hemodynamics of Systoilc BP greater than 100mmhg and diastolic BP greater than 60mmhg

Exclusion criteria

Exclusion criteria: 1)Previous history of atrial tachyarrhythmias and antiarrhythmic drug use, 2)Permanent, Paroxysmal atrial fibrillation of unknown duration where also excluded, 3)Hemodynamic instability- a systolic blood pressure (SBP) of less than 90 mmHg and indicated for electrical cardioversion. 4)Patients will also be excluded if their Atrial fibrillation had a wide-complex ventricular response (potential Wolff-Parkinson-White preexcitation syndrome, 5)Chronic Kidney Disease. 6)Severe valvular heart diseases. 7)Sick sinus syndrome, or rhythm other than Atrial fibrillation.

Design outcomes

Primary

MeasureTime frame
Conversion to normal sinus rhythm and rate control.Timepoint: 1 hour, 4 hours, 8 hours, 12 hours and 24 hours

Secondary

MeasureTime frame
Therapeutic response (referred to as resolution time), Differences in characteristics between magnesium responders and non-responders, To assess if there has been a reduction in the requirement for antiarrhythmic medicationsTimepoint: 1 hour, 4 hours, 8 hours, 12 hours and 24 hours

Countries

India

Contacts

Public ContactRISHWANTH RAJA P M

Sri Ramachandra Institute of Higher Education and Research

hod.criticalcare@sriramachandra.edu.in8870767379

Outcome results

None listed

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