Exploring the link between glycoxidation and arterial health in at-risk individuals
Official title: Multimodal Vascular Phenotyping and Target-Organ Damage Using Vascular Imaging, Glyco-Oxidative Biomarkers, and Photoplethysmography in Adults at Increased Cardiovascular Risk: The GlycOxiTOD Observational Registry
Run by Complejo Hospitalario Universitario de Santiago · NCT06325800 · Data updated 2026-11-12
This study looks at how certain changes in the body might affect artery health in people at risk for heart problems to see if they can spot early signs of damage.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Complejo Hospitalario Universitario de Santiago Academic / other |
| Locations | 1 site (Santiago de Compostela, A Coruña) |
| Status | Recruiting |
| Started | January 10, 2024 |
| Main results expected | March 31, 2031 |
| Study ends | December 31, 2035 |
| Registry record updated | August 5, 2026 |
| Trial ID | NCT06325800 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are non-smoking adults over 18 years old with moderate to high cardiovascular risk.
✕Probably not a fit
Patients with diabetes mellitus or established cardiovascular disease will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study investigates the relationship between glycoxidation, arterial biomechanics, and target organ damage in individuals with moderate to high cardiovascular risk. It aims to understand how glycation and oxidative stress affect arterial health and contribute to vascular aging. The study will collect demographic, clinical, and anthropometric data from non-smoking participants over 18 years old, who do not have diabetes or established cardiovascular disease. By analyzing these factors, researchers hope to uncover insights into the mechanisms of cardiovascular risk and potential early indicators of target organ damage.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and early detection of cardiovascular risks, potentially guiding preventive strategies.
How similar studies have gone: While the specific focus on glycoxidation and arterial biomechanics in healthy individuals is novel, related studies have shown success in understanding cardiovascular risk factors.
Who can join: the full rules
Show full inclusion / exclusion criteria
INCLUSION CRITERIA * Age 18 years or older. * Written informed consent to participate in the registry. * Undergoing cardiovascular risk or hypertension assessment in a primary-prevention setting. * At least one of the following cardiovascular risk conditions: * Confirmed hypertension requiring specialist cardiovascular assessment. * A SCORE2 estimated 10-year cardiovascular risk of 2% or higher in participants aged 40 to 69 years, when SCORE2 is applicable. * A SCORE2-OP estimated 10-year cardiovascular risk of 2% or higher in participants aged 70 to 89 years, when SCORE2-OP is applicable. * Type 2 diabetes with at least moderate cardiovascular risk according to SCORE2-Diabetes in participants within its validated age range, or according to guideline-defined clinical risk criteria when SCORE2-Diabetes is not applicable. * Chronic kidney disease confirmed for at least 3 months, defined by an estimated glomerular filtration rate below 60 mL/min/1.73 m², a urinary albumin-to-creatinine ratio of 30 mg/g or higher, or another persistent marker of kidney damage. * Hypertension-mediated target-organ damage or subclinical atherosclerotic vascular disease documented by clinical, laboratory, imaging, or functional assessment. * Confirmed or probable familial hypercholesterolemia. * For participants aged 18 to 39 years or older than 89 years, a documented major cardiovascular risk condition, such as hypertension, type 2 diabetes, chronic kidney disease, familial hypercholesterolemia, or target-organ damage. EXCLUSION CRITERIA * Inability or unwillingness to provide written informed consent. * Established clinical cardiovascular disease requiring secondary-prevention management, including previous myocardial infarction, acute coronary syndrome, stroke, transient ischemic attack, coronary or peripheral revascularization, symptomatic peripheral artery disease, or other established symptomatic cardiovascular disease. * Acute or clinically unstable illness that prevents completion of the baseline registry assessment. * A medical, technical, cognitive, or logistical condition that prevents completion of the minimum required registry procedures.
Where it's running
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Complejo Hospitalario Universitario de Santiago de Compostela
Santiago de Compostela, A Coruña, Spain Recruiting
Study contacts
- Study coordinator: Nestor Vazquez-Agra, PhD
- Email: nestor.vazquez.agra@sergas.es
- Phone: 0034981951256
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.