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Qatar Cardiometabolic Retrospective Cohort-Analysis Using Artificial Intelligence

Qatar Cardiometabolic Retrospective Cohort-Analysis Using Artificial Intelligence

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07515807
Acronym
QCRC-AI
Enrollment
10000
Registered
2026-04-07
Start date
2026-07-16
Completion date
2030-07-16
Last updated
2026-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndromes (ACS), Artifical Intelligence, Cardio Vascular Disease, Pre Diabetes, Type 2 Diabetes

Brief summary

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.

Detailed description

This study combines retrospective and prospective designs. Retrospective: We use past electronic medical records to identify participants and collect baseline information from their initial visit (using their code or health card number). Prospective: From that starting point, we follow the same participants forward in time, updating data every two years and recording new outcomes (mortality, cardiovascular events, rehospitalizations, treatment-related outcomes) at planned checkpoints (approximately 6 months, 1 year, and 2 years). New eligible participants identified in later data extractions are added and followed in the same manner. Because we only observe and record participants existing records and outcomes without assigning interventions, the study is observational.

Interventions

None listed

Sponsors

Weill Cornell Medical College in Qatar
Lead SponsorOTHER
Hamad Medical Corporation
CollaboratorINDUSTRY

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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%

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of 3-point Major Adverse Cardiovascular Events (MACE) in Acute Coronary Syndrome Patients5 yearsComposite 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.
Incidences of 2-point Major Adverse Cardiovascular Events (MACE) in Heart Failure Patients5 yearsComposite 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.

Secondary

MeasureTime frameDescription
Major Adverse Cardiovascular Events5 yearsMACE - Major Adverse Cardiovascular Events
Unstable angina requiring hospitalization5 years
Arrhythmic events5 years
Coronary revascularization5 years
Post-Percutaneous Coronary Intervention (PCI) or Coronary Artery Bypass Grafting (CABG) complications (stent/graft thrombosis or repeat revascularization)5 years
Development or progression of valvular heart disease (aortic or mitral stenosis/regurgitation)5 years
New-onset diabetes mellitus5 years
Change in glycated Hemoglobin A1c (HbA1c)5 years
Newly diagnosed medical or surgical conditions not present at baseline5 years

Countries

Qatar

Contacts

CONTACTCharbel Abi Khalil Prof
cha2022@qatar-med.cornell.edu+ 974 4492 8484
PRINCIPAL_INVESTIGATORCharbel Abi Khalil

Weill Cornell Medicine-Qatar

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 22, 2026