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Clinical Trials/NCT03463148
NCT03463148
Completed
Not Applicable

Validation of a Sensor for Non-Invasive Measurement of Vital Signs, Hemodynamic Parameters and Time-Dependent Physiological Waveforms

Baxter Healthcare Corporation1 site in 1 country136 target enrollmentOctober 24, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
CHF
Sponsor
Baxter Healthcare Corporation
Enrollment
136
Locations
1
Primary Endpoint
Fluids
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Subjects will be measured with both a sensor and a reference device

Detailed Description

Subjects will participate in a study measuring a single set of paired values. In this case, measurements will take roughly 2-30 minutes to complete, and will involve: 1) attaching the sensor on the subject; 2) attaching one or more reference devices to the subject; 3) making measurements with both the sensor and reference device, either simultaneously or sequentially; and 4) collecting and analyzing the paired value.

Registry
clinicaltrials.gov
Start Date
October 24, 2017
End Date
April 19, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subject is at least 18 (eighteen) years of age at screening.
  • Subject and/or legally authorized person/representative is willing to undergo the Informed Consent process prior to enrollment in the study.
  • Subject selection will not be based on age, height, or weight.
  • Subject is a candidate for this study based on the PI's opinion and knowledge of the subject's condition as well as the features of the investigational device tested during the study.

Exclusion Criteria

  • Subject is participating in another clinical study that may affect the results of either study.
  • Subjects that are pregnant will not be included in the study.
  • Subject is unable or not willing to wear electrode patches as required for a period of up to 168 hours.
  • Subject is considered by the Principal Investigator to be medically unsuitable for study participation.

Outcomes

Primary Outcomes

Fluids

Time Frame: 3-36 Months

Observation of fluid measurement from Sensor (ohms)

Comparison of Blood Pressure Measurement from Sensor with Human Auscultation measurement of Blood Pressure.

Time Frame: 3-36 Months

Comparison of Blood Pressure Measurement from Sensor with Human Auscultation measurement of Blood Pressure. Specifically, Systolic Blood Pressure and Diastolic Blood Pressure with units of millimeters of mercury (mmHg) will be compared.

Heart Rate Variability

Time Frame: 3-36 Months

Observation of heart rate variability from Sensor (milliseconds)

Respiration Rate

Time Frame: 3-36 Months

Observation of respiration rate from Sensor (breaths/min)

Heart Rate

Time Frame: 3-36 Months

Observation of heart rate measurement from Sensor (beats/min)

Study Sites (1)

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