Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
110000 participants
OBSERVATIONAL
1998-01-31
Brief Summary
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Detailed Description
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The registry uses advanced information technology that integrates personal computerized community and hospital records, data from laboratory tests, dispensed medications, physiological signals, radiological images, and reports from investigations and procedures.
Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Cardiovascular Disease Patients
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Ischemic Heart Disease,MI,non-MI,congestive heart failure,peripheral vascular disease, cerebrovascular disease CVA,TIA,patients with first AMI diagnosis from community physicians if they were hospitalized for lasting at least 3 days during a 30-day period prior to diagnosis.
* Patients with prior coronary artery bypass grafting(CABG) or percutaneous coronary intervention (PCI), using relevant Current Procedural Terminology (CPT) codes
Exclusion Criteria
* Patients whose primary physician reported that the patient is CHD-free providing adequate medical records
ALL
No
Sponsors
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Maccabi Healthcare Services, Israel
OTHER
Responsible Party
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Principal Investigators
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Gabriel Chodick, PHD
Role: STUDY_DIRECTOR
Head,Epidemiology & Database Reseaech Unit, Medical Division, Maccabi H.S
Locations
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Maccabi Healthcare Services
Tel Aviv, , Israel
Countries
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References
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Shalev V, Chodick G, Goren I, Silber H, Kokia E, Heymann AD. The use of an automated patient registry to manage and monitor cardiovascular conditions and related outcomes in a large health organization. Int J Cardiol. 2011 Nov 3;152(3):345-9. doi: 10.1016/j.ijcard.2010.08.002. Epub 2010 Sep 9.
Other Identifiers
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cvdregistry
Identifier Type: REGISTRY
Identifier Source: secondary_id
MACCVREG1
Identifier Type: -
Identifier Source: org_study_id
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