Coronary Heart Disease Clinical Trial
— MEASURE-cBP1Official title:
Non-invasive Automated Central Blood Pressure Measurements Using Oscillometric Pulse Wave Analysis - Comparison With Invasive Reference Values
| Verified date | December 2017 |
| Source | Universitätsmedizin Mannheim |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
There is growing evidence that central blood pressure is a better predictor of hypertensive
end-organ damage and cardiovascular outcome than routine brachial readings.
The investigators aimed to evaluate the accuracy of a novel device for the non-invasive
determination of central blood pressure based on automated oscillometric radial pulse wave
analysis.
| Status | Completed |
| Enrollment | 106 |
| Est. completion date | October 30, 2017 |
| Est. primary completion date | May 31, 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - patients undergoing routine coronary angiography Exclusion Criteria: - inability to give informed consent - hemodynamic instability |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Universitätsmedizin Mannheim |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | agreement of systolic central blood pressure measurements | 15 minutes | ||
| Primary | agreement of diastolic central blood pressure measurements | 15 minutes |
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