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ENROLLING BY INVITATION
NCT05441696

Study for the Evaluation of a Non-invasive Hemodynamic Measurement in Heart Failure Patients

Sponsor: Nihon Kohden

View on ClinicalTrials.gov

Summary

Track changes in non-invasive central venous pressure across hospital stay and relationship with readmission

Official title: Pilot Study for the Evaluation of EzCVP in Heart Failure Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

65

Start Date

2022-06-01

Completion Date

2026-09-29

Last Updated

2024-12-27

Healthy Volunteers

No

Interventions

DEVICE

ezCVP measurement

* Measuring device: non-FDA-cleared patient monitor (740E, Zoe Medical, MA, US), which has software to measure ezCVP. * Sensor: an FDA-cleared pulse oximeter sensor for adults (K012891: DS-100A, Nellcor, CA, US). * Cuff: an FDA-cleared NIBP cuff for adults (K080342: YP-713T, YP-714T or TP-715T, Nihon Kohden Corporation, Tokyo, Japan).

Locations (2)

Veterans Affairs Hospital

Palo Alto, California, United States

Stanford Medical Center

Stanford, California, United States