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Clinical Trials/NCT03096119
NCT03096119
Completed
Not Applicable

A Study to Define the Distribution of Type of Hypertension in Asia by Blood Pressure Monitoring at Home (Asia BP@Home)

Jichi Medical University1 site in 1 country1,462 target enrollmentApril 6, 2017
ConditionsHypertension

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypertension
Sponsor
Jichi Medical University
Enrollment
1462
Locations
1
Primary Endpoint
Distribution rate based on the home BP of the patients.
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Blood pressure variability (BPV) is being increasingly recognized as an important influence on hypertension outcomes as well as a risk factor for other cardiovascular (CV) events. However, in Asia there is a current lack of awareness of BPV and its significance on patient outcomes. Furthermore, there is ongoing debate on the role of home blood pressure (HBP) monitoring in managing hypertension patients and uncertainty on how best to integrate it into clinical practice.

Therefore, we conduct Asia BP@Home study to assess HBP control status in each Asian country and develop an Asian consensus and Asia-specific treatment for hypertension.

Detailed Description

Blood pressure variability (BPV) is being increasingly recognized as an important influence on hypertension outcomes as well as a risk factor for other cardiovascular (CV) events. However, in Asia there is a current lack of awareness of BPV and its significance on patient outcomes. Furthermore, there is ongoing debate on the role of home blood pressure (HBP) monitoring in managing hypertension patients and uncertainty on how best to integrate it into clinical practice. The main purpose of this study is to: * Assess HBP control status in each Asian country * Develop an Asian consensus and Asia-specific treatment for hypertension * Improve the management of hypertension in Asia by encouraging patients to monitor HBP

Registry
clinicaltrials.gov
Start Date
April 6, 2017
End Date
March 31, 2018
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kazuomi Kario

Professor & Chairman

Jichi Medical University

Eligibility Criteria

Inclusion Criteria

  • Age \>= 20 years
  • Subjects with stable medication (\> 3 months) diagnosed as hypertension
  • Subjects have been thoroughly informed about this registry and signed an Informed Consent Form.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Distribution rate based on the home BP of the patients.

Time Frame: 7 days or more blood pressure measurement

Distribution rate based on the home BP of the patients who are defined as: * Masked morning hypertension * White-coat hypertension * Poorly controlled hypertension * Well controlled hypertension

Study Sites (1)

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