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Clinical Trial Summary

The purpose the research is to prospectively demonstrate agreement between EHR and ambulatory blood pressure monitor (ABPM) derived blood pressure variability (BPV), as well as the feasibility of reducing BPV using a data-driven pharmacotherapeutic approach. To this end, this is a feasibility study that will make use of the Cedars-Sinai Health System including the Medical Delivery Network and the clinics of all practitioners who use the same EHR.


Clinical Trial Description

The primary research procedures are: assessment of blood pressure variability (BPV) using ABPM compared to EHR derived values; and to assess feasibility of a data driven pharmacotherapy intervention to reduce BPV among high BPV patients. As part of an option sub-study, participants may wear a single lead ECG patch to record skin sympathetic nerve activity (SKNA), which has been previously correlated with changes in blood pressure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06012487
Study type Interventional
Source Cedars-Sinai Medical Center
Contact Joseph Ebinger
Phone 3104230925
Email cda-research@cshs.org
Status Not yet recruiting
Phase Phase 1
Start date May 1, 2024
Completion date December 31, 2024

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