Observational Study of the Sleuth Implantable ECG Monitoring System

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00717106

Acronym

OBSERV-ECG

Enrollment

250

Registered

2008-07-16

Start date

2008-07-31

Completion date

Unknown

Last updated

2009-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrhythmia, Fainting, Presyncope, Syncope

Keywords

ILR, ECG monitoring, cardiac arrhythmia, syncope, presyncope, fainting

Brief 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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Time to diagnosis	one year

Countries

United States

Outcome results