Observational Study of the Sleuth Implantable ECG Monitoring System

NCT00717106 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 250

Last updated 2009-05-05

No results posted yet for this study

Summary

The purpose of this study is to obtain information on real-world device performance clinical assessments and clinical outcomes of patients receiving the Sleuth Implantable ECG Monitoring System.

Conditions

  • Syncope
  • Presyncope
  • Fainting
  • Cardiac Arrhythmia

Sponsors & Collaborators

  • Transoma Medical

    lead INDUSTRY

Principal Investigators

  • Wim Stegink · Transoma Medical

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-07-31

Countries

  • United States

Study Locations

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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 NCT00717106 on ClinicalTrials.gov