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Sponsors and Collaborators: |
Brigham and Women's Hospital Aetna, Inc. |
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Information provided by: | Brigham and Women's Hospital |
ClinicalTrials.gov Identifier: | NCT00566774 |
The objective of this randomized trial is to evaluate the effect of providing full prescription drug coverage (i.e. no co-pays, co-insurance or deductibles) for statins, beta-blockers, angiotensin converting enzyme inhibitors and angiotensin II receptor blockers to patients recently discharged from hospital after acute myocardial infarction.
Condition | Intervention | Phase |
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Myocardial Infarction Coronary Artery Disease |
Other: Full drug coverage Other: Usual coverage |
Phase IV |
Study Type: | Interventional |
Study Design: | Health Services Research, Randomized, Single Blind (Investigator), Active Control, Parallel Assignment, Efficacy Study |
Official Title: | Post-Myocardial Infarction Free Rx Event and Economic Evaluation (Post-MI FREEE) Trial: a Randomized Evaluation of First-Dollar Coverage for Post-MI Secondary Preventive Therapies |
Estimated Enrollment: | 7500 |
Study Start Date: | November 2007 |
Estimated Study Completion Date: | May 2010 |
Arms | Assigned Interventions |
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1: Experimental |
Other: Full drug coverage
Patients randomized to first-dollar coverage will have their pharmacy benefits changed so that they have no out-of-pocket costs for any beta-blocker, angiotensin converting enzyme inhibitor (ACEI) or angiotensin II receptor blocker (ARB) antagonist, or statin for every subsequent prescription after randomization. All co-pays and co-insurance will be waived at the point of care (i.e. pharmacy) as will any contribution that the cost of these drugs contributes to a patient's deductible
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2: Active Comparator |
Other: Usual coverage
Patients randomized to usual coverage will have no change in their existing benefits
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Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Michele Toscano, MS | 860-273-5970 | ToscanoM@aetna.com |
United States, Connecticut | |
Aetna Inc | Recruiting |
Hartford, Connecticut, United States, 06156 | |
Contact: Michele Toscano, MS 860-273-5970 ToscanoM@aetna.com | |
Sub-Investigator: Troyen Brennan, MD, MPH, JD |
Principal Investigator: | Niteesh K Choudhry, MD, PhD | Brigham and Women's Hospital/Harvard Medical School |
Responsible Party: | Brigham and Women's Hospital/Harvard Medical School ( Niteesh K. Choudhry, Assistant Professor ) |
Study ID Numbers: | 2007-P-000847/1 |
Study First Received: | November 30, 2007 |
Last Updated: | November 30, 2007 |
ClinicalTrials.gov Identifier: | NCT00566774 |
Health Authority: | United States: Institutional Review Board |
myocardial infarction secondary prevention health insurance cost-sharing |
Arterial Occlusive Diseases Heart Diseases Myocardial Ischemia Vascular Diseases Ischemia Arteriosclerosis Angiotensin II |
Coronary Disease Necrosis Aspirin Neoplasm Metastasis Infarction Myocardial Infarction Coronary Artery Disease |
Neoplasms Neoplastic Processes Pathologic Processes Cardiovascular Diseases |