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Clinical Trials/NCT04665011
NCT04665011
Completed
Not Applicable

Validation of Indicor Photoplethysmography (PPG) Valsalva Pulse Response vs Non-invasive Blood Pressure

Vixiar Medical, Inc.1 site in 1 country121 target enrollmentDecember 14, 2020
ConditionsHeart Failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure
Sponsor
Vixiar Medical, Inc.
Enrollment
121
Locations
1
Primary Endpoint
pulse amplitude ratio
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This study designed is compare the pulse response to the Valsalva maneuver between a photoplethysmography sensor (PPG) and non-invasive blood pressure sensor for the purpose of validating the PPG methodology in deriving a value for the Valsalva pulse response. The aim is to show that the PPG method captures the same phase responses as the blood pressure monitor and the primary outcome is the correlation between pulse amplitude ratios for the pulse at the end of the Valsalva to an average baseline pulse.

Detailed Description

With both a photoplethysmography (PPG; Indicor, Vixiar Medical,. Baltimore, MD) and non-invasive blood pressure (Caretaker, Caretaker Medical, Charlottesville, VA) sensors in place on the index and middle fingers, respectively, each patient will be asked to perform three mild, 10-sec Valsalva maneuvers with at least 45 seconds between. Pulse recordings will be collected from each device to compare phases of the Valsalva pulse response including pulse amplitude changes and baseline movement. The primary outcome is the correlation between pulse amplitude ratios for the pulse at the end of the Valsalva to an average baseline pulse.

Registry
clinicaltrials.gov
Start Date
December 14, 2020
End Date
January 28, 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Clinically stable adults, including heart failure patients visiting an outpatient clinic

Exclusion Criteria

  • Atrial flutter or atrial fibrillation with an irregular ventricular response
  • Significant atrial or ventricular ectopy
  • History of paradoxical emboli
  • Hypertrophic obstructive cardiomyopathy
  • Known intracardiac shunt
  • Known severe aortic valve stenosis
  • Known severe mitral valve stenosis
  • History of embolic CVA
  • Myocardial infarction within one week of intended Indicor testing
  • Uncontrolled hypertension (systolic BP \>160mmHg or diastolic BP\>100mmHg)

Outcomes

Primary Outcomes

pulse amplitude ratio

Time Frame: 5 minutes

The correlation between PPG-based and non-invasive blood pressure pulse amplitude ratio during a Valsalva maneuver.

Secondary Outcomes

  • Phases of valsalva pulse response(5 minuntes)

Study Sites (1)

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