MedTrace Logo

Evaluation of a Mobile Cardiac Outpatient Telemetry System Versus Standard Loop Event Monitor

NCT00295204 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2006-08-03

No results posted yet for this study

Summary

Comparing the arrhythmia diagnostic yield of MCOT as compared to standard loop event monitors in patients presenting with palpitations, syncope or near syncope occurring less frequently than every 24 hours. Patients randomized and are enrolled for 30 days. Prior testing required: 24 hours of non diagnostic monitoring,

Conditions

  • Syncope
  • Pre-Syncope
  • Palpitations

Sponsors & Collaborators

  • Cardionet

    lead INDUSTRY

Principal Investigators

  • Stephen Rothman, MD · Mainline Arrhythmia and Cardiology Associates

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-04-30
Completion
2006-10-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00295204 on ClinicalTrials.gov