Actively Recruiting
A Registry Study on the Action of Controlling Ambulatory Blood Pressure to Target in Ten Thousand Patients
Led by Yan Li · Updated on 2025-01-06
10000
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the management of hypertension, a common and serious cardiovascular disease that can lead to stroke, heart attack, and heart failure. This study focuses on the use of 24-hour ambulatory blood pressure monitoring (ABPM) as recommended by European guidelines to improve hypertension diagnosis and treatment. The research aims to gather nationwide data on hypertensive patients in China to assess differences in cardiovascular outcomes based on ABPM control. Participants in this observational study have hypertension and use antihypertensive medications. They undergo 24-hour ABPM with validated devices, and their clinical information, including disease history and recent blood biochemical tests, is collected. The study promotes the clinical use of ambulatory monitoring to better detect various hypertension types and evaluate treatment effects over time. Throughout the study, researchers record major cardiovascular and cerebrovascular events for up to three years from enrollment. They also track clinic and ambulatory blood pressure control rates, as well as the occurrence of white-coat and masked hypertension. Participants provide consent and data while continuing their usual care. The study aims to improve hypertension management and reduce related health risks in the population.
CONDITIONS
Brief Title
A Registry Study on the "Action of Controlling Ambulatory Blood Pressure to Target in Ten Thousand Patients"
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-80 years old
- Clinical diagnosed hypertension with use of antihypertensive drugs
- Performed 24-hour ambulatory blood pressure monitoring with validated equipment
- Willing to provide disease history and blood biochemical test data within 6 months
- Signed informed consent
You will not qualify if you...
- Not using antihypertensive drugs
- Hospitalized hypertension patients
- Non-compliant patients
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 3 years
Participants are monitored to collect data on blood pressure control and cardiovascular events over time.
Regular monitoring visits as per routine care
Trial Site Locations
Total: 1 location
1
Ruijin Hospital
Shanghai, Shanghai Municipality, China, 200025
Actively Recruiting
Research Team
Y
Yan Li, Professor
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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