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Cryptogenic Stroke Study

Not Applicable
Conditions
Cryptogenic Stroke
Registration Number
NCT00861133
Lead Sponsor
Transoma Medical
Brief Summary

The purpose of this study is to determine whether the Sleuth Implantable Loop Recorder will enhance detection of latent atrial fibrillation in patients after cryptogenic stroke.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Recent stroke (within 30 days) as defined by who has a sudden onset of focal neurological deficits presumed vascular etiology and lasting more than 24 hours.
  • Negative brain image for hemorrhagic stroke
  • In sinus rhythm at time of enrollment
Exclusion Criteria
  • Know history of atrial fibrillation
  • Previous implanted cardiac device (ppM or ICD)
  • Serious illness making it unlikely to survive one year
  • Known secondary cause of stroke

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Incidence of atrial fibrillation at one year from Sleuth implantation.One Year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

The Ohio State University

🇺🇸

Columbus, Ohio, United States

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