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Clinical Trials in Denmark / NCT07781371
Starting soon Observational

A Retrospective Real-World Cohort Study

NCT07781371 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2026-08-20
Last updated
2026-08-24

Condition(s) studied

ObesityType 2 Diabetes (T2D)PrediabetesCardiovascular Disease (CVD)DyslipidemiaMetabolic Dysfunction-associated Steatotic Liver Disease (MASLD)Chronic Kidney Disease (CKD)

Investigational drug(s) / intervention(s)

No treatment given

No treatment given: No treatment given

Study summary

The primary objectives are to determine the prevalence and overlap of major cardiometabolic diseases, identify multimorbidity clusters, and characterize demographic, clinical, laboratory, and treatment patterns across the cohort and relevant subgroups. This study is based on anonymized electronic health record (EHR) data and spanning January 2022 to December 2025. EHR will be extracted from participants of Acibadem hospital network in Turkey. Participants received routine clinical care according to physician discretion. Index date will be defined by the first diagnosis of cardiometabolic conditions.

Follow-up period will include at least one year of to allow description of long-term outcomes. It will extend until the end of study, last recorded encounter, or death.

Eligibility

Sex
ALL
Min age
12 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Participants aged above or equal to 12 years at index date. * Participants with international classification of diseases (ICD-10) coded diagnosis or secondary criteria for either diabetes (type 2 diabetes, pre-diabetes), overweight, obesity, metabolic dysfunction-associated steatotic liver disease (or non-alcoholic fatty liver disease), cardiovascular disease (arterial hypertension, ischemic heart disease, myocardial infarction, heart failure, cerebrovascular disease (including stroke and transient ischemic attack), atherosclerosis, atrial fibrillation), chronic kidney disease, dyslipidemia. * At least one healthcare encounter within 12 months prior to index date (pre-index) to ensure availability of baseline data. Exclusion Criteria: * None.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Novo Nordisk Investigational Site Copenhagen Denmark

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07781371 on ClinicalTrials.gov ↗ ← All trials in Denmark