The investigators aim to evaluate subjects at high risk of future development of hypertension, those with a family history of hypertension and/or that already have high normal(SBP 120-139 mmHg or DBP 80-89 mmHg) blood pressure. The investigators plan to investigate whether these subjects have the same markers (such as microscopic protein in the urine or C-reactive protein in the blood) in the blood and urine that people with high blood pressure have, and whether they are improved before and after taking the beta-blocker nebivolol.
Age range
18 Years – 50 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Aortic Systolic Blood Pressure (SBP)
Timeframe: Basline (visit 1) and 8 weeks (visit 2)
Aortic Diastolic Blood Pressure (DBP)
Timeframe: Basline (visit 1) and 8 weeks (visit 2)
Aortic Mean Arterial Pressure (MAP)
Timeframe: Basline (visit 1) and 8 weeks (visit 2)
Aortic Pulse Pressure
Timeframe: Basline (visit 1) and 8 weeks (visit 2)
Aortic Augmentation Pressure
Timeframe: Basline (visit 1) and 8 weeks (visit 2)
Aortic Augmentation Index for Heart Rate
Timeframe: Basline (visit 1) and 8 weeks (visit 2)
Pulse Wave Velocity
Timeframe: Basline (visit 1) and 8 weeks (visit 2)
Heart Rate, Beats Per a Minute
Timeframe: Basline (visit 1) and 8 weeks (visit 2)