Cardiac Disease Clinical Trial
Official title:
Mobile Advanced Multi-Parameter Reporting in Patients Wearing a Novel Device: Utilization During Cardiac Rehabilitation
Advanced remote multi-parameter reporting during cardiac rehabilitation (MAPS-III). The primary purpose of this observational study is to collect baseline information of cardiac rehabilitation usage in the US for post-myocardial infarction (MI) patients with EF > 35% while wearing the ZOLL AMS device for 30 to 60 days. Secondary data on biometrics, arrhythmias, symptoms, and healthcare utilization will provide additional background information on this population during the early post-MI cardiac rehabilitation period.
To collect baseline data on cardiac rehabilitation usage (referrals and completion) in recent post-MI patients with EF > 35%.To collect data on AMS-derived biometric data (e.g. HR, activity) and arrhythmias, and subject-reported symptoms, beta blocker/ivabradine usage (dose/changes) and cardiovascular events. The participating centers will enroll consenting subjects in a sequential manner to avoid preferential selection of patients to participate in the study. Subjects will be consented by the center study staff, and if eligible will wear the FDA-cleared AMS device for 30-60 days. Subject demographic information and clinical history will be obtained at the time of enrollment. During the study period, the prescribing physician-investigator will be blinded to AMS data. Final subject follow-up will be at 3 months. A sample size of 150 subjects is estimated in order to have 100 subjects with at least 30 days of AMS use for analysis. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT05490303 -
HeartGuide: Preliminary Study
|
N/A | |
| Completed |
NCT05070819 -
Atrial Natriuretic Peptide in Assessing Fluid Status
|
N/A | |
| Not yet recruiting |
NCT04538469 -
Absent Visitors: The Wider Implications of COVID-19 on Non-COVID Cardiothoracic ICU Patients, Relatives and Staff
|
||
| Not yet recruiting |
NCT04511403 -
Prevalence of Oral Mucosal Alterations In a Sample of Egyptian Patients With Cardiovascular Diseases: A Hospital- Based Cross-Sectional Study
|
||
| Completed |
NCT02697760 -
The CZT Dynamic Myocardial Perfusion Imaging
|
||
| Terminated |
NCT05157568 -
Pilot Randomized Clinical Trial of Live-streamed Cardiovascular Rehabilitation
|
N/A | |
| Not yet recruiting |
NCT04160845 -
Non-invasive Forehead Skin Temperature in Cardiac Surgery
|
||
| Completed |
NCT04500912 -
Comparison of the Supraflex Cruz 60 Micron Versus the Ultimaster Tansei 80 Micron in HBR PCI Population
|
N/A | |
| Not yet recruiting |
NCT06438159 -
Impact of Mindfulness-Based Stress Reduction Meditation Practice on Patients After Cardiac Rehabilitation.
|
N/A | |
| Recruiting |
NCT06154473 -
Assessment of Patients Undergoing Cardiac Surgery and Admitted to the Intensive Care Unit
|
||
| Not yet recruiting |
NCT05877755 -
Validation of Multi-contrast, High-resolution Cardiac Magnetic Resonance Imaging
|
N/A | |
| Completed |
NCT03394859 -
Electronic Medical Records and Genomics (eMERGE) Phase III
|
||
| Recruiting |
NCT05055830 -
Opportunistic PK/PD Trial in Critically Ill Children (OPTIC)
|
||
| Recruiting |
NCT04374799 -
Heparin vs Placebo for Cardiac Catheterization
|
Phase 3 | |
| Completed |
NCT03174106 -
Longterm Follow-up of Cardiac Patients With an Smartphone-Application
|
N/A | |
| Recruiting |
NCT05531253 -
Respired Gases in Patients Post Cardiac Surgery
|
||
| Recruiting |
NCT04609228 -
Cardiac Surgery Outcomes in Blood-transfusion Acceptors and no Acceptors
|
||
| Recruiting |
NCT06149143 -
Cardiac Performance System Data Collection Study - Minnesota
|
||
| Recruiting |
NCT05725655 -
Hot Water Immersion After Myocardial Infarction
|
N/A | |
| Recruiting |
NCT06073509 -
Atrial Fibrillation and Other Cardiac Arrhythmias and Diseases After Radiotherapy for Breast Cancer : Watch Your HeaRT
|