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Study to Gather Information to What Extent Patients Follow the Treatment Regimen of Low-dose Aspirin for Primary and Secondary Prevention of Diseases of the Heart and Blood Vessels (PALACE)

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Bayer

Status

Completed

Conditions

Unstable Angina
Stroke (Including Ischaemic Stroke and Transient Ischaemic Attack)
Myocardial Infarction
Ischaemic Heart Disease
Angina

Treatments

Drug: Acetylsalicylic Acid (Aspirin, BAYE4465)

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

This study aims to gather information to what extent patients follow the treatment regimen of low-dose aspirin for primary and secondary prevention of diseases of the heart and blood vessels. Researcher will collect information about the percentage of time a patient has access to the medication, how long patients continue with the medication and of the proportion of patients who switch from dual-antiplatelet therapy (including low-dose aspirin) to a single antiplatelet therapy. The study will make use of secondary healthcare data sources converted in to Observational Medical Outcomes Partnership (OMOP) common data model within the Observational Health Data Sciences and Informatics (OHDSI) network.

Enrollment

99,999 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged ≥18 years

  • Patients will be selected if they have at least two prescriptions for low-dose aspirin (75-100 mg) between 2008 and 2018 for either:

    • Primary prevention of CVD This is defined as patients who have no history of CVD any time prior to initiation of low-dose aspirin treatment are presumed to use for primary CVD prevention
    • Secondary prevention of CVD This is defined as patients who have a history of CVD any time prior to initiation of low-dose aspirin treatment
  • Patients with at least two prescriptions of low-dose aspirin with a dosage of 75-100mg within the first year of the index date.

  • Restricted to patients with observation for at least 12 months before and 12 after the index date.

Exclusion criteria

  • Prescription of low-dose aspirin in 12 months before the index date.

Trial design

99,999 participants in 1 patient group

Low-dose aspirin users
Description:
Patients who receive low-dose aspirin (75-100mg) for either the primary or secondary prevention of cardiovascular disease (CVD).
Treatment:
Drug: Acetylsalicylic Acid (Aspirin, BAYE4465)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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