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Possibilities of Interpreting the Night-to-Day Ratio Specified by 24-hour Blood Pressure Monitoring — ABPM  

Cardiovascular Diseases Clinical Trial

Official title:
Seven-day Ambulatory Blood Pressure Monitoring and CAVI in the Prevention of Cardiovascular Diseases

Clinical Trial Summary

Specify the risk rate of incorrect patient classification based on night-to-day ratio specification from singular 24-h ABPM in comparison to the results of 7-day ABPM monitoring

Clinical Trial Description

The subjects in the study are divided into 4 groups: group 1 (40 healthy men and women without exercise); group 2 (40 healthy exercise-training men and women); group 3 (40 patients with ischemic coronary artery disease without exercise); and group 4 (51 patients with ischemic coronary artery disease following cardiovascular rehabilitation). The subject of the evaluation is the percentage rate of incorrect subject classification (dipper, non-dipper, extreme dipper, and risers) based on the mean blood pressure values for 7 days and from seven independent 24-hour cycles (the mean value mode). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05264090
Study type Interventional
Source St. Anne's University Hospital Brno, Czech Republic
Contact
Status Completed
Phase N/A
Start date June 20, 2018
Completion date June 20, 2021
View Details
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