Monitoring Arrhythmia Patients (IMPACT)
Completed
- Conditions
- Arrhythmias
- Registration Number
- NCT00919568
- Lead Sponsor
- Corventis, Inc.
- Brief Summary
Prospective, multicenter, non-randomized study to determine the performance of NUVANT Mobile Cardiac Telemetry system in arrhythmia detection.
- Detailed Description
Arrhythmia patients will be externally monitored. The collected information will be used to evaluate the NUVANT MCT system.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 28
Inclusion Criteria
- 18 years of age or older
- Patients undergoing remote ambulatory electrocardiographic monitoring
Exclusion Criteria
- Is participating in another clinical study that may confound the results of this study
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What are the molecular mechanisms of arrhythmia detection using the NUVANT Mobile Cardiac Telemetry system in NCT00919568?
How does the NUVANT MCT system compare to standard-of-care telemetry in arrhythmia monitoring efficacy?
Which biomarkers correlate with arrhythmia risk in patients monitored by the NUVANT system in NCT00919568?
What adverse events are associated with long-term cardiac telemetry using NUVANT in arrhythmia patients?
Are there alternative monitoring technologies to NUVANT MCT for detecting atrial fibrillation and other arrhythmias?
Trial Locations
- Locations (1)
Dr. Bedi
🇺🇸Steubenville, Ohio, United States
Dr. Bedi🇺🇸Steubenville, Ohio, United States