- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06992284
- Original Trial
A Prognostic Study for Patients With Cardiovascular Disease in Niigata
A Prognostic Study Using Health Insurance Claim for Patients With Cardiovascular Disease in Niigata
The goal of this observational study is to investigate the prognosis of cardiovascular disease in Niigata Prefecture.
Specifically, it aims to clarify the current status of medical treatment for cardiovascular disease patients in regional cities in Japan, where the population is aging.
With patient consent, the study will track long-term medical treatment progress using health insurance claim data recorded in Japan's unique social security system.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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-
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Niigata, Japan, 951-8114
- Niigata University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Individuals aged 18 or older at the time of enrollment (regardless of gender).
- Individuals who have been hospitalized in the cardiology department of a participating medical institution.
- Individuals covered by Japan's National Health Insurance (NHI) or the Late-stage Elderly Medical Care System, which provide health coverage for self-employed individuals, retirees, and the elderly.
Exclusion Criteria:
- Individuals who are unable to obtain consent from themselves or their legally authorized representatives.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The rate of deterioration in care dependency levels as defined by Japan's Long-Term Care Insurance system
Time Frame: through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
through study completion, an average of 1 year
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024-0250
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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