Qatar Cardiometabolic Retrospective Cohort-Analysis Using Artificial Intelligence

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorWeill Cornell Medical College in Qatar

About this trial

Cardiovascular disease is the leading cause of death worldwide, and individuals with diabetes or other cardiometabolic conditions are at increased risk of adverse cardiovascular outcomes. Although advances in prevention and treatment have reduced cardiovascular events globally, cardiometabolic disease continues to represent a significant health burden, particularly in regions with high diabetes prevalence. In Qatar and other Gulf Cooperation Council countries, the prevalence of diabetes and obesity is increasing, contributing to a high proportion of participants presenting with acute coronary syndrome who have type 2 diabetes or prediabetes. This observational study will use electronic medical record data from patients hospitalized at the Heart Hospital with acute coronary syndrome and a concomitant diagnosis of diabetes or prediabetes. The study will assess trends in cardiovascular risk factors and cardiovascular events, including readmission and mortality. An artificial intelligence component will be used to develop and validate machine learning based risk prediction models to forecast adverse cardiovascular outcomes in participants with cardiometabolic disease. These models will integrate clinical, biochemical, imaging, and other non-invasive data routinely collected during participants care to identify predictors of cardiovascular events.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18

Qatari and Arab participants

Participants admitted for Acute Coronary Syndrome (ACS) or Acute Heart Failure (AHF)

Metabolic disease: Diabetes (HbA1C ≥ 6.5% or any HbA1C if a patient is on an antidiabetic agent) or pre-diabetes: 5.7% ≤ HbA1c ≤ 6.4%

Disqualifiers

Non-Qatari or non-Arab participants

Non-diabetic: HbA1C < 5.7%

This chart review involves no direct interaction with individuals. Prisoners are not a focus of this study, and incarceration status is not identifiable in the records reviewed.

Trial population

Participants admitted at Hamad Medical Corporation for Acute Coronary Syndrome (ACS) or Acute Heart Failure (AHF).

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Incidence of 3-point Major Adverse Cardiovascular Events (MACE) in Acute Coronary Syndrome Patients

Composite endpoint defined as the occurrence of cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke. Events will be identified using electronic medical records, hospital admission data, and follow-up assessments during the study period. These outcomes will serve as endpoints for the development and validation of predictive machine learning models.

Time frame
5 years
2

Incidences of 2-point Major Adverse Cardiovascular Events (MACE) in Heart Failure Patients

Composite endpoint defined as cardiovascular death or hospitalization for heart failure. Events will be ascertained through hospital records, clinical documentation, and follow-up data collection. These outcomes will be used as endpoints for predictive model development and validation.

Time frame
5 years

Secondary outcomes

1

Major Adverse Cardiovascular Events

MACE - Major Adverse Cardiovascular Events

Time frame
5 years
2

Unstable angina requiring hospitalization

Time frame
5 years
3

Arrhythmic events

Time frame
5 years
4

Coronary revascularization

Time frame
5 years

Other outcomes

Sponsors and contacts

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Weill Cornell Medical College in Qatar

Lead sponsor

Hamad Medical Corporation

Collaborator

This trial is not recruiting at the moment. You can still explore other options: