Mobile Cardiac Telemetry and Advanced Multi-Parameter Monitoring in PatientS Wearing a Novel Device With Biometric Based Medications Changes

Zoll Medical Corporation62 enrolled

Overview

To determine the associations among biometric data and previously reported medication changes in the original MAPS study

1. Each center that previously reported making a medication change in a MAPS patient based on biometric information will complete a case report form detailing the rhythm, symptom, medication and dosage change, and which biometric(s) were used to make this decision. 2. Follow up at 6 months will be determined for all patients to assess the impact of the medication change.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Cardiac Arrhythmia

Interventions

Arrhythmia Management System (AMS)DEVICE

Retrospective collection of data related to subjects who participated in the MAPS 90D0234 study and had a medication change reported will wearing the AMS device.

Eligibility

Sex: ALLMin age: 21 Years

Medical Language ↔ Plain English

Inclusion Criteria: * those that completed the MAPS study and that had medication changes based wholly or in part on biometric information. Exclusion Criteria: * Those patients from the MAPS study that did not have medication changes.

Locations (8)

Cardiovascular Institute of Central Florida

Ocala, Florida, United States

First Coast Heart & Vascular Center

Saint Augustine, Florida, United States

Jackson Heart Clinic

Jackson, Mississippi, United States

PharmaTex Research

Amarillo, Texas, United States

Outcomes

Primary Outcomes

Association Between Arrhythmia Biometric and Medication Change

Clinical Case Report Form

Time frame: 1 Day

Association Between Subject-Reported Symptom Biometric and Medication Change

Clinical Case Report Form

Time frame: 1 Day

Association Between Subject Wellness Biometric and Medication Change

Clinical Case Report Form

Time frame: 1 Day

Association Between Subject Adverse Event and Medication Change

Clinical Case Report Form

Time frame: 1 Day

Association Between Subject Status and Medication Change

Clinical Case Report Form

Time frame: 1 Day

Association Between Subject Hospital Events and Medication Change

Clinical Case Report Form

Time frame: 1 Day

Association Between Subject Clinical Events and Medication Change

Clinical Case Report Form

Time frame: 1 Day

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.