Homocysteine and Early Diastolic Dysfunction in Newly Diagnosed Hypertension
Condition(s) studied
Investigational drug(s) / intervention(s)
Homocysteine Measurement and Echocardiography: Peripheral venous blood sampling for plasma homocysteine measurement and comprehensive transthoracic echocardiography including diastolic function assessment and strain analysis.
Study summary
This prospective single-center observational study aims to evaluate the relationship between elevated plasma homocysteine levels and early echocardiographic abnormalities in patients with newly diagnosed essential hypertension. Adult patients diagnosed with essential hypertension within the previous 6 months will undergo clinical assessment, ambulatory blood pressure monitoring, electrocardiography, laboratory testing, and comprehensive transthoracic echocardiography including diastolic function assessment and strain analysis when image quality is adequate. Participants will be classified according to plasma homocysteine level using, and patients with elevated and normal homocysteine levels will be compared with respect to diastolic dysfunction and left ventricular and left atrial global longitudinal strain parameters. Clinical, laboratory, and echocardiographic data will also be used to develop a machine-learning based model for prediction of H-type hypertension.
Eligibility
Primary outcome measure(s)
- Presence of Early Left Ventricular Diastolic Dysfunction — Baseline assessment at enrollment
Presence of early left ventricular diastolic dysfunction based on predefined echocardiographic diastolic function criteria assessed by transthoracic echocardiography at baseline, compared between patients with elevated homocysteine levels and normal homocysteine levels.
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Necmettin Erbakan University Meram Faculty of Medicine | Konya | Meram | Recruiting |
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Other trials for the same condition
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 NCT07480265 on ClinicalTrials.gov ↗ ← All trials in Turkey