Blood Pressure Clinical Trial
Official title:
Comparison of Arterial Tonometry Sensor (BPro) With Standard Oscillometric Blood Pressure Monitoring Device (Oscar 2) for Ambulatory Use
Verified date | October 2019 |
Source | Pontificia Universidad Catolica de Chile |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study aims at comparing the values of the blood pressure measurements obtained during 24 hours by an arterial tonometry device (BPRo) and a standard oscillometric blood pressure monitoring device (Oscar 2) under ambulatory conditions
Status | Completed |
Enrollment | 33 |
Est. completion date | July 30, 2019 |
Est. primary completion date | July 30, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 25 Years and older |
Eligibility |
Inclusion Criteria: - Able to give informed consent Exclusion Criteria: - Difference in blood pressure between the arms higher than 10 mmHg |
Country | Name | City | State |
---|---|---|---|
Chile | Institute for Biological and Medical Engineering | Santiago | Metropolitana |
Lead Sponsor | Collaborator |
---|---|
Pontificia Universidad Catolica de Chile | Comisión Nacional de Investigación Científica y Tecnológica |
Chile,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Difference in systolic blood pressure taken simultaneously by BPro and Oscar 2 devices | Mean of the absolute differences in systolic blood pressure (mmHg) taken simultaneously by BPro and Oscar 2 devices at 15 minutes intervals during the day and 30 minutes intervals during the night for a period of 24 hours | 24 hours | |
Primary | Difference in diastolic blood pressure taken simultaneously by BPro and Oscar 2 devices | Mean of the absolute differences in diastolic blood pressure (mmHg) taken simultaneously by BPro and Oscar 2 devices at 15 minutes intervals during the day and 30 minutes intervals during the night for a period of 24 hours | 24 hours |
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