- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07313137
Antiplatelet Use in Dementia Subtypes
December 17, 2025 updated by: ZEHRA SARIKAYA DEMIRBAS, Gulhane Training and Research Hospital
Antiplatelet Use in All-Cause Dementia and Dementia Subtypes Among Older Adults: A Population-Based Cohort Study
This population-based retrospective cohort study aimed to evaluate the appropriateness of antiplatelet therapy use among older adults with all-cause dementia and across different dementia subtypes.
Medical records of patients aged 65 years and older who were evaluated at a tertiary-level geriatric outpatient clinic were reviewed.
Dementia subtypes were classified according to internationally accepted diagnostic criteria.
Patterns of antiplatelet use were assessed in accordance with current guideline recommendations.
The study sought to determine the appropriateness of antiplatelet use across dementia subtypes and to describe real-world prescribing practices in this population.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
683
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
The study population consists of older adults aged 65 years and older with a diagnosis of dementia who were evaluated in a tertiary-level geriatric outpatient clinic.
Description
Inclusion Criteria:
- Age 65 years and older.
- Diagnosis of dementia based on internationally accepted diagnostic criteria.
- Evaluation at a tertiary-level geriatric outpatient clinic.
Exclusion Criteria:
- Patients with incomplete or inaccessible medical records.
- Individuals with missing data on antiplatelet therapy use.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Dementia cohort
This cohort includes older adults aged 65 years and older diagnosed with dementia who were evaluated in a tertiary geriatric outpatient clinic.
No intervention was assigned, as this is a retrospective observational study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Appropriateness of antiplatelet therapy use
Time Frame: At baseline (first geriatric outpatient clinic visit)
|
Assessment of the appropriateness of antiplatelet therapy use according to current guideline recommendations among older adults with dementia.
|
At baseline (first geriatric outpatient clinic visit)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2016
Primary Completion (Actual)
March 1, 2025
Study Completion (Actual)
March 1, 2025
Study Registration Dates
First Submitted
December 17, 2025
First Submitted That Met QC Criteria
December 17, 2025
First Posted (Actual)
December 31, 2025
Study Record Updates
Last Update Posted (Actual)
December 31, 2025
Last Update Submitted That Met QC Criteria
December 17, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GTRH-ANTIPL-DEM-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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