About this trial
The primary aim is to determine whether non-dipping status is associated with adverse repolarization markers and impaired myocardial mechanics compared to dipper hypertensive patients. Secondary analyses will compare these findings among resistant vs. non-resistant and controlled vs. uncontrolled hypertensive groups. This study may provide new insights into the prognostic significance of blood pressure dipping patterns in hypertensive patients.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults ≥18 years old
Diagnosed with essential hypertension
Completed 24-hour ambulatory blood pressure monitoring (ABPM)
Availability of good-quality 12-lead ECG
Disqualifiers
Body mass index (BMI) > 34.9 kg/m²
Atrial fibrillation or atrial flutter
Use of QT-prolonging medications
End-stage renal disease or liver failure
Trial population
Adult patients (≥18 years) with essential hypertension attending the Cardiology Department at Assiut University Heart Hospital. All participants will undergo 24-hour ambulatory blood pressure monitoring, electrocardiography, and echocardiography to classify them into dipper and non-dipper groups
Trial design
Other
Prospective
Treatments tested in this trial
Nocturnal Blood Pressure Dipping
Other interventionPatients will be classified as dippers (≥10% nocturnal BP fall) or non-dippers (\<10% nocturnal BP fall) based on 24-hour ambulatory blood pressure monitoring.
Treatment groups
Trial outcomes
Primary outcomes
Effect of nocturnal BP dipping on ECG markers of ventricular repolarization
Evaluation of QTc, QT dispersion, and Tp-Te interval in dipper vs. non-dipper hypertensive patients, correlated with echocardiographic changes
Secondary outcomes
Repolarization and echocardiographic changes in resistant vs. non-resistant hypertension
Comparison of ECG and echocardiographic markers between resistant and non-resistant hypertensive groups
Locations
Sponsors and contacts
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