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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COMPLETED
NA
115 participants
INTERVENTIONAL
2009-01-31
2013-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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1
Standard care
No interventions assigned to this group
2
Educational session with pharmacist, nutritionist, and cardiac rehabilitation nurse
Education
Educational session with pharmacist, nutritionist, and cardiac rehabilitation nurse
Interventions
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Education
Educational session with pharmacist, nutritionist, and cardiac rehabilitation nurse
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Jeffrey Kramer, MD
OTHER
Responsible Party
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Jeffrey Kramer, MD
CTS SURGEON
Principal Investigators
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Jeffrey Kramer, MD
Role: PRINCIPAL_INVESTIGATOR
University of Kansas Medical Center
Locations
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University of Kansas Medical Center
Kansas City, Kansas, United States
Countries
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Other Identifiers
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11562
Identifier Type: -
Identifier Source: org_study_id
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