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Clinical Trial Summary

The main purpose of this study in healthy participants is to find out whether the traditional ambulatory blood pressure monitor (ABPM) and newer wearable devices (EmbracePlus smartwatch device, Biobeat chest patch device, and Aktiia wrist device) will accurately pick up changes in blood pressure caused by 2 different medications (propranolol and pseudoephedrine). The study will last about 29 days excluding the screening period of 28 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05692869
Study type Interventional
Source Eli Lilly and Company
Contact This is a single site clinical trial. 1-877-CTLILLY (1-877-285-4
Phone 1-317-615-4559
Email ClinicalTrials.gov@Lilly.com
Status Not yet recruiting
Phase N/A
Start date January 18, 2023
Completion date March 3, 2023

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