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Completed
NCT05723744
Anonymized Data Collection From the CS6BP for Heart Arrythmias Measurements
Conditions: Heart Arrythmias
Sex: All
Ages: 18 Years – N/A
Phase: NA
Enrollment: 47
Sponsor: CardiacSense Ltd.
Location: Israel
Summary
The purpose of this clinical study is to collect data simultaneously with the CS6BP watch sensors during EPS in order to characterize different evoked arrhythmias and record Blood Pressure during the procedures that blood pressure is collected by an automated cuff.
Eligibility Criteria
Inclusion Criteria:Age of eighteen (18) year and aboveIn clinical need for electrophysiology study (standalone or before ablation procedure) and/or Subjects with AVB who are candidates for pacemaker implantationAbility and willingness to sign an informed consent formExclusion Criteria:Patients with significant co morbidities (assessed by the clinician at screening only):Mechanically ventilated patients Mechanical circulation (LVAD, IABP, ECMO)Subjects who are currently enrolled in another clinical investigation in which the intervention might compromise the safety of the subject's participation in this studySubjects with PPG SNR <100 indicated by the CS6BP deviceWomen who are pregnant or breastfeedingSubjects with had deformity banning from wearing the device
Source: ClinicalTrials.gov (NCT05723744). StuddyBuddy aggregates publicly available trial information.
