Validation of Pulse Waveform Analysis-based Continuous Noninvasive Blood Pressure Measurement Sensor

Tampere University Hospital30 enrolled

Overview

The study aims to define the sensitivity and specificity of a novel continuous noninvasive blood pressure monitor.

A novel continuous noninvasive blood pressure monitor is compared to invasive arterial measurement at postoperative care unit after a planned operation. Monitor captures also saturation and ECG, which are compared to traditional monitoring.

Study Type

INTERVENTIONAL

Allocation

Purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Enrollment

Conditions

Blood Pressure

Interventions

Study Monitor usedDEVICE

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * subjected to operative treatment with the need for invasive blood pressure measurement * spontaneous ventilation * able to give informed consent Exclusion Criteria: * denial by patient * pacemaker

Locations (1)

Tampere University Hospital

Tampere, Finland

Outcomes

Primary Outcomes

Relationship between invasive and noninvasive blood pressure measurement

comparability of study monitor systolic, diastolic and mean blood pressure to invasive blood pressure measurement

Time frame: 2 hours of continuous measurement at PACU

Secondary Outcomes

Relationship between study monitor Sp02 measurement and current sp02 measurement

comparability of measurements at several timepoints recorded as 10s intervals

Time frame: 2 hours of continuous measurement at PACU

Data from ClinicalTrials.gov

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