- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06281054
Acute Myocardial Infarction in Cancer Patients
March 12, 2025 updated by: Joo Myung Lee, Samsung Medical Center
Risk and Clinical Outcomes of Acute Myocardial Infarction in Patients With Cancer: A Nationwide Study
Using national health insurance service database, current study aim to evaluate the risk and prognosis of acute myocardial infarction in cancer patients and to find the optimal treatment strategy for acute myocardial infarction that can improve long-term prognosis.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
This study will be conducted using Korean National Health Insurance Service database.
Patients who were diagnosed with cancer from 2002 to 2021 will be included in the study.
Using the selected patients, current study will analyze the incidence and prognosis of acute myocardial infarction in cancer patients and the prognosis according to the treatment method for acute myocardial infarction will be compared.
Primary outcome will be all-cause death.
Secondary outcomes will be myocardial infarction, revascularization, hospitalization for heart failure, stroke, and clinically relevant bleeding.
Study Type
Observational
Enrollment (Estimated)
4500000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Gwangju, Korea, Republic of
- Chonnam National University Hospital, Chonnam National University Medical School
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients who were diagnosed with cancer from 2002 to 2021 will be considered in the study.
Among these patients, those diagnosed with acute myocardial infarction after the diagnosis with cancer will be included in the study.
Description
Inclusion Criteria:
- Patients diagnosed with cancer between 2002 and 2021
- Patients who were diagnosed with acute myocardial infarction after cancer diagnosis
Exclusion Criteria:
- Patients who died during period of cancer diagnosis
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 |
Intervention / Treatment |
|---|---|
|
Revascularized Group
Cancer patients with diagnosis of acute myocardial infarction that was treated with PCI or CABG
|
Performing PCI or CABG
|
|
Medical Group
Cancer patients with diagnosis of acute myocardial infarction that was treated with medical treatment only
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
All-cause death
Time Frame: 2-years after diagnosis of acute myocardial infarction
|
All-cause death which was obtained from death certification collected by Statistics Korea at the Ministry of Strategy and Finance of South Korea
|
2-years after diagnosis of acute myocardial infarction
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Myocardial infarction
Time Frame: 2-years after diagnosis of acute myocardial infarction
|
Myocardial infarction is defined as presence of the diagnostic codes (ICD-10 I21, I22) in the primary position during hospitalization
|
2-years after diagnosis of acute myocardial infarction
|
|
Revascularization
Time Frame: 2-years after diagnosis of acute myocardial infarction
|
Percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG)
|
2-years after diagnosis of acute myocardial infarction
|
|
Hospitalization for heart failure
Time Frame: 2-years after diagnosis of acute myocardial infarction
|
Heart failure events requiring hospitalization defined as presence of the diagnostic codes (I110, I130, I132, I255, I420, I425-I429, I43, I50, I971) in the primary position during hospitalization
|
2-years after diagnosis of acute myocardial infarction
|
|
Stroke
Time Frame: 2-years after diagnosis of acute myocardial infarction
|
Stroke is defined as ischemic stroke (ICD-10 I63, I64) or intracranial hemorrhage (ICD-10 I60-62), combined with the codes of diagnostic brain imaging.
|
2-years after diagnosis of acute myocardial infarction
|
|
Clinically relevant bleeding
Time Frame: 2-years after diagnosis of acute myocardial infarction
|
Bleeding requiring hospitalization or transfusion
|
2-years after diagnosis of acute myocardial infarction
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Joo Myung Lee, MD, MPH, PhD, Samsung Medical Center
- Principal Investigator: Seung Hun Lee, MD, PhD, Chonnam National University Hospital
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)
January 1, 2002
Primary Completion (Actual)
December 31, 2021
Study Completion (Estimated)
December 31, 2025
Study Registration Dates
First Submitted
February 20, 2024
First Submitted That Met QC Criteria
February 20, 2024
First Posted (Actual)
February 28, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 12, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SMC2023-12-027
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
This is National Health Insurance Data Analysis.
Therefore, sharing the original patient-level data is not possible under regulation by the Korean government.
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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