Massive study tracks cost and use of heart attack meds in US and germany
NCT ID NCT07610577
First seen Jun 27, 2026 · Last updated Jul 10, 2026 · Updated 2 times
Summary
This study analyzes data from over 377,000 people who had a heart attack and were prescribed blood thinners (clopidogrel, ticagrelor, or prasugrel) in Germany and the United States between 2011 and 2024. Researchers aim to describe how often each drug is used and how much it costs over time. The goal is to provide insights into prescribing patterns and healthcare spending, not to test a new treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- clopidogrel, prasugrel, ticagrelor (blood thinners)
- What this could lead to
- If successful, this could help doctors and policymakers understand how these blood thinners are prescribed and what they cost, potentially leading to more affordable and effective heart attack care.
- What could go wrong
- This is an observational study using existing data, so it cannot prove cause and effect. Results may not apply to all patients or healthcare systems.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
377,753 people
The number who actually took part.
- Started
-
Nov 2025
- Finished
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May 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adults aged ≥18 years with acute myocardial infarction who initiated outpatient treatment with clopidogrel, ticagrelor, or prasugrel.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
This study uses a series of descriptive observational analyses conducted using German and US healthcare claims data, the CMS Open Payments database, and Medicare Part D prescribing data by national provider identifier. Patient-level analyses will use new-user cohort study designs conducted separately in German and US administrative healthcare claims databases. These analyses will evaluate temporal trends in the age- and sex-standardized initiation of clopidogrel, ticagrelor, and prasugrel among adults initiating outpatient P2Y12 inhibitor therapy after acute myocardial infarction and describe these trends in the context of the evolving evidence base and guideline recommendations. In addition, patient-level analyses will assess temporal trends in 12-month treatment costs, as well as population-level trends in major adverse cardiovascular events and bleeding-related hospitalizations among P2Y12 inhibitor initiators in Germany. Separate US-based analyses will evaluate industry payments associated with ticagrelor and prasugrel reported in the CMS Open Payments database and provider-level prescribing patterns according to receipt of ticagrelor-associated industry payments using linked Medicare Part D prescribing data. Eligible cohort entry dates for patient-level analyses will range from 2011 through 2024. PATIENT-LEVEL COHORT ANALYSES Inclusion Criteria * Adults aged ≥18 years * Acute myocardial infarction * Initiation of outpatient treatment with clopidogrel, ticagrelor, or prasugrel Exclusion Criteria * Prior use of clopidogrel, ticagrelor, or prasugrel * Initiation of more than one study drug on the cohort entry date * Missing age or sex information * Insufficient baseline claims enrollment TICAGRELOR-TO-PRASUGREL COST-SAVING ANALYSIS IN THE UNITED STATES Eligibility Criteria * Adults aged ≥18 years * Acute myocardial infarction * Initiation of outpatient treatment with ticagrelor INDUSTRY PAYMENT ANALYSIS IN THE UNITED STATES Eligibility Criteria * General and research payment records in the CMS Open Payments database * Ticagrelor or prasugrel listed as the associated drug PROVIDER-LEVEL PRESCRIBING ANALYSIS Eligibility Criteria * US Medicare Part D providers * \>10 ticagrelor or prasugrel claims during both the baseline period (2020-2021) and outcome period (2022-2023).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Brigham and Women's Hospital
Boston, Massachusetts, 02120, United States
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Other studies related to the condition(s) this trial covers.
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