Clinical Trial

Homocysteine and Early Diastolic Dysfunction in Newly Diagnosed Hypertension

Study acronym: HHT-EDD
Recruiting
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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.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-03-14.
Trial Details
NCT Number NCT07480265
Lead Sponsor Necmettin Erbakan University
Conditions Hypertension (HTN), Hyperhomocysteinemia, Diastolic Dysfunction
Enrollment 500 participants
Start Date 2025-06-02
Primary Completion 2027-12 (estimated)
Study Completion 2028-03 (estimated)
Updated on ClinicalTrials.gov 2026-03-24