Implantable Cardioverter Defibrillator Clinical Trial
Official title:
Barriers to Use of Remote Monitoring in Patients With Implantable Cardioverter Defibrillators
Verified date | January 2018 |
Source | Yale University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine whether a teaching intervention can help increase the use of remote monitors in patients with implantable cardioverter defibrillators.
Status | Completed |
Enrollment | 20 |
Est. completion date | October 2014 |
Est. primary completion date | April 2014 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Received a Medtronic implantable cardioverter defibrillator (ICD) at Yale Electrophysiology, between January 2007 and June 2012 - ICD is compatible with Carelink, Medtronic's remote monitoring system Exclusion Criteria: - Less than 18 years of age - From a vulnerable population - Incompetent/suffers from dementia - Non-English speaking |
Country | Name | City | State |
---|---|---|---|
United States | Yale Electrophysiology | New Haven | Connecticut |
Lead Sponsor | Collaborator |
---|---|
Yale University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of remote Transmissions of data using remote monitor made by patient | 6 months |
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