CompletedNot Applicable

CareLink® Network Evaluation

Poland176 participantsStarted 2010-01

Plain-language summary

The purpose of the study is to demonstrate the value of the Medtronic CareLink® Network in clinical practice in the country specific healthcare setting.

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients who have an implanted Medtronic ICD, CRT-D device that is supported by the Medtronic CareLink® Network * Patients have to sign the Medtronic CareLink® "Statement of Privacy Principles" and the "Evaluation Data Protection Statement" documents Exclusion Criteria: * Patients with exclusion criteria required by local law * Patient is anticipated to demonstrate poor compliance (for example, mental disturbances)

What they're measuring

Comparison of Remote Device Check and In-clinic Device Assessment

Timeframe: Baseline to max. 12 months

Trial details

NCT IDNCT01023022

SponsorMedtronic Cardiac Rhythm and Heart Failure

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2013-03

Results submitted2014-08-22

View on ClinicalTrials.gov More Heart Failure trials