Comparison of Continuous Sternal ECG Patch Monitors (Carnation and Zio) Trial
Completed
Conditions studied: Syncope, Presyncope, Atrial Fibrillation, Supraventricular Tachycardia
In brief
The purpose of this research is to test the clinical value of a new P-wave sensitive recording vector compared to a standard ECG limb lead II vector from similar easy-to-use long-term cardiac rhythm monitoring patch systems, the Carnation TM Ambulatory Monitoring (CAM) System and the Zio-XT iRhythm. The P-wave is a critical aspect of the electrocardiogram. The purpose of this study is to see if the P-wave centric focus of the CAM system improves arrhythmia diagnosis.
Key facts
- Study ID
- NCT02952781
- Run by
- EvergreenHealth
- People needed
- 30
- Starts
- 2016-10-01
- Expected to finish
- 2017-01-01
- Last updated by the study team
- 2017-03-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female
- Written informed consent
- Patients with one or more of the following:
- Syncope of uncertain etiology; or
- Pre-syncope of uncertain etiology; or
- Palpitations of uncertain etiology; or
- Management of known AF/SVT patients
You may not qualify if…
- Any dermatitis or infected skin over the sternum (Carnation patch) or left upper anterior thorax (Zio patch).
- A sternal or thoracic incision that extends under the patch within 3 months from the date of enrollment.
- Cognitive deficits that would interfere with the subject's ability to give informed consent or perform study testing
Where it is running
- EvergreenHealth Heart and Vascular Care — Kirkland, Washington, United States
Full record on ClinicalTrials.gov
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