Actively Recruiting
Registry Study on Control Nocturnal Hypertension to Reach the Target (CONTROL-NHT)
Led by Shanghai Institute of Hypertension · Updated on 2025-01-06
4500
Participants Needed
1
Research Sites
369 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Ambulatory blood pressure monitoring (ABPM) has become an important tool for diagnosing hypertension by measuring blood pressure throughout daily activities and sleep. This research focuses on the significance of nocturnal blood pressure, which has been found to better predict fatal and non-fatal cardiovascular events like stroke and heart attack, especially in patients on medication. The study aims to understand how controlling nighttime blood pressure affects cardiovascular outcomes in patients with nocturnal hypertension. The study collects nationwide prospective data on patients diagnosed with nocturnal hypertension who are using antihypertensive drugs. Participants have undergone 24-hour ABPM with validated equipment to confirm elevated nighttime blood pressure. The research involves monitoring participants over time to compare cardiovascular event rates based on how well their nocturnal blood pressure is controlled. Participants will be followed for up to three years, during which researchers will record the time to any fatal or non-fatal cardiovascular event. The study requires participants to provide medical history and biochemical test results within six months and to consent to the study. This long-term observation will help assess the impact of nighttime blood pressure management on heart health and stroke risk.
CONDITIONS
Official Title
Registry Study on "Control Nocturnal Hypertension to Reach the Target "
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 50-79 years old
- Clinical diagnosis of hypertension with use of antihypertensive drugs
- Nocturnal hypertension defined as nocturnal systolic blood pressure 64 130 mmHg and/or nocturnal diastolic blood pressure 64 80 mmHg
- 24-hour ambulatory blood pressure monitoring performed with validated equipment
- Willing to provide disease history and blood biochemical test data from within 6 months
- Signed informed consent
You will not qualify if you...
- Not using antihypertensive drugs
- Hospitalized hypertension patients
- Patients who are non-compliant
AI-Screening
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Trial Site Locations
Total: 1 location
1
Ruijin Hospital
Shanghai, Shanghai Municipality, China, 200025
Actively Recruiting
Research Team
Y
Yan Li, MD,PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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