Observational Study of the Sleuth Implantable ECG Monitoring System

Status unconfirmed

Conditions studied: Syncope, Presyncope, Fainting, Cardiac Arrhythmia

In brief

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.

Key facts

Study ID

NCT00717106

Run by

Transoma Medical

People needed

250

Starts

2008-07-01

Last updated by the study team

2009-05-05

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with clinical syndromes or situations at increased risk of cardiac arrhythmias
• Patients who experience transient symptoms that may suggest a cardiac arrhythmia

You may not qualify if…

• Patients that have had a myocardial infarction (MI) < 30 days prior to implant

Where it is running

• Piedmont Hospital — Atlanta, Georgia, United States
• Western Maryland Health Systems — Cumberland, Maryland, United States
• Cardiology Consultants of East Michigan — Lapeer, Michigan, United States
• St. Luke's - Roosevelt — New York, New York, United States
• SUMMA-NEOCS Health Systems — Akron, Ohio, United States
• Main Line Health - Lankenau Hospital — Wynnewood, Pennsylvania, United States
• Center for Cardiac Arrhythmias — Houston, Texas, United States
• Morgantown Internal Medicine Group — Morgantown, West Virginia, United States

Full record on ClinicalTrials.gov

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