Wearable Cardiac Monitor to Enhance Detection of Arrhythmia Recurrence After Catheter Ablation of Atrial Fibrillation
NCT06564012
Arrhythmias, Cardiac, Atrial Fibrillation
View Trial DetailsNCT Number: NCT06103305
the aim of the study is to early diagnose and early proper mangment of those patients who have palpitations specially of cardiac origin
Trial opening soon.
Get Notified18 year–80 year
All sexes
Observational
Palpitation : are one of the most common presentations to general practice, and while they are usually benign, they may also have life-threatening significance. Palpitations have been estimated to account for 16% of general practice presentations and are the second most common presentation to cardiologists after chest pain.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
The present study will be conducted on patients with Palpitations "without intently selected certain gender" and had 18 years old or more
Exclusion criteria
patients refusing study will be excluded.
Time frame: 30 days
Mortality during 30 days follow up
Time frame: 0 days
Admission to hospital from the Emergency Department
Time frame: 0 days
Admission to the Intensive Care Unit or High Dependency Unit from the Emergency Department
Contact information is provided by the study sponsor or research team.
Assiut University
Other
Risk Stratifications for Patients Come With Palpitations in Assiut and Suez Canal University Hospitals
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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