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Medtronic Observational Study in the "Real World" of Implantable Electronic Cardiac Devices

NCT01189630 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 3500

Last updated 2011-03-30

No results posted yet for this study

Summary

The Observational Study in the "Real World" of Implantable Electronic Cardiac Devices will enable the construction of an electronic database with local access to clinical information, which will collect and disseminate epidemiologic data on demography, cardiovascular mortality and morbidity, and potential risk factors for a selected group of patients. These clinical variables will be analyzed against the data, as based in the programming of devices and the diagnostics. Approved descriptive statistics and analyses will be made available via Internet. The study will describe statistical indexes on sub-groups representing more than 10% of total of datasets.

The study will be open to include any patient that had a Medtronic electronic device implanted, pacemakers, ICD, ICD with CRP. The study will be also adapted for devices implanted in the present and for devices to be implanted in patients in the future.

Conditions

Sponsors & Collaborators

  • Medtronic Comercial Ltda.

    lead INDUSTRY

Principal Investigators

  • Roberto Takeda, MD · Medtronic Comercial

Eligibility

Min Age
18 Years
Max Age
95 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-12-31
Completion
2015-12-31

Countries

  • Brazil

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01189630 on ClinicalTrials.gov