Accuracy of Non-Invasive Blood Pressure Measurement in Adults

Withdrawn

• Conditions: Hypertension; Hypotension

• Registration Number: NCT01183741
• Lead Sponsor: Sotera Wireless, Inc.

Brief Summary

The purpose of this study is to compare the accuracy of the Sotera ViSi, an investigational device, to auscultation (measurement with a cuff) in determining systolic and diastolic blood pressure (BP) in adult subjects.

Detailed Description

This study is a single-center blinded study that will enroll approximately 150 adult subjects. Trained auscultators will perform the standard auscultation BP measurements. They will be blinded to each other's measurements and from the ViSi measurements.

The study population will be randomized into two groups based on the side of the blood pressure measurement: the left arm group (LAG) and the right arm group (RAG).

The randomization ratio of the LAG and RAG will be 1:1. There will be forced stratification in order to ensure that the study subjects meet the required arm circumference and blood pressure distributions as specified in the SP10:2008 and ISO 81060-2:2009(E) standards.

Study Timeline

• Study First Submitted: 2010-08-13
• Study First Submitted QC: 2010-08-16
• Study First Posted: 2010-08-18
• Study Start: 2010-09
• Primary Completion: 2010-10
• Study Completion: 2010-10
• Status Verified: 2011-06
• Last Update Submitted: 2011-06-21
• Last Update Posted: 2011-06-22

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

• Subject is greater than 12 years of age at the time of screening.
• Subject's upper arm circumference is between 20cm and 55cm.
• Subject is willing to undergo the Informed Consent process prior to enrollment in the study.
• Subject is willing and able to participate for up to 60 minutes.

Exclusion Criteria

• Subject is participating in another clinical study that may interfere with the results of this study.
• Subject is unable to have a blood pressure measurement taken from either arm for any reason.
• Subject is evaluated by the Investigator and found to be medically unsuitable for participation in this study.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

Scripps Clinic Rancho Bernardo; 🇺🇸 San Diego, California, United States