Evaluation of Ambulatory Monitoring of Patients After High-risk Acute Coronary Syndrome Using Two Different Systems: Biomonitor-2 and Kardia Mobile
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Arrhythmias Cardiac
- Atrial Fibrillation
- Heart Diseases
- Syncope
- Tachycardia
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Prevention
Participation Requirements
- Age
- Between 18 years and 85 years
- Gender
- Both males and females
Description
The objective of the study is to evaluate the efficacy of monitoring after discharge of patients with high-risk acute coronary syndrome.
The objective of the study is to evaluate the efficacy of monitoring after discharge of patients with high-risk acute coronary syndrome.
Tracking Information
- NCT #
- NCT03940066
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Felipe Rodríguez Entem, MD, PhD Hospital Universitario Marqués de Valdecilla Principal Investigator: José M De la Torre Hernández, MD, PhD Hospital Universitario Marqués de Valdecilla
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