BIO|STREAM.ICM Obesity
NCT04198220
Arrhythmias, Cardiac, Atrial Fibrillation
Castrovillari, Italy
View Trial DetailsNCT Number: NCT04732728
The LUX-Dx PERFORM Study had two primary objects which were (1) to characterize, in a general patient population, the utilization of the remote programming feature of the Boston Scientific (BSC) Insertable Cardiac Monitor (ICM) device and (2) to collect data to characterize the performance of arrhythmia detection algorithms. Data was also collected to characterize the ICM system related safety events.
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Notify Me18 year and older
All sexes
Observational
Heart Center Research, LLC, Huntsville, Alabama, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
The following inclusion criterion is applicable for patients participating in the Holter study:
Exclusion criteria
The following exclusion criteria are applicable for patients participating in the Holter study:
Time frame: 30 days
Time frame: 12 months
Boston Scientific Corporation
Industry
Acronym: LUX-Dx PERFORM
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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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