ClinicalTrials.Veeva

Menu

Comparison of Arterial Tonometry Sensor With Standard Oscillometric Blood Pressure Monitoring Device

P

Pontificia Universidad Catolica de Chile

Status

Completed

Conditions

Blood Pressure

Treatments

Device: BPro

Study type

Interventional

Funder types

Other

Identifiers

NCT03997461
170706006

Details and patient eligibility

About

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

Full description

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. Measurements will be taken at 15 minutes intervals during the day and 30 minutes intervals during the night.

Enrollment

33 patients

Sex

All

Ages

25+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Able to give informed consent

Exclusion criteria

  • Difference in blood pressure between the arms higher than 10 mmHg

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

33 participants in 1 patient group

BPro vs Oscar 2
Experimental group
Description:
Blood pressure measurement with BPro and Oscar 2 simultaneously during 24 hours under ambulatory conditions
Treatment:
Device: BPro

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems