CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 879 enrolled
Drug / intervention
ViSi devicedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04574908
NCT04574908N/ACompleted
CompareCT.gov

A Pilot Trial of Continuous Portable Postoperative Hemodynamic And Saturation Monitoring On Hospital Wards

Wake Forest University Health Sciences·interventional·Posted Oct 5, 2020·Updated May 21, 2024

In Brief

A clinical study evaluating ViSi device for Hemodynamic Instability and Respiratory Complications of Care. Completed, enrolled 879 participants across 1 site.

Detailed Summary

The study team will collect data for this study from participants who are having surgery and recovering postoperatively on 2 pre-designated hospital units. The study team will use vital signs data from a portable device that participants wear on their wrists as well as conventional vital signs data that is collected when a health care provider comes into their room and collect this information. A substudy is also being performed with the distribution of surveys to the nursing staff on the floors who are utilizing the ViSi hemodynamic monitors within our institution.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHemodynamic Instability, Respiratory Complications of Care
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedOct 5, 2020
Enrollment StartOct 7, 2020
Primary CompletionOct 6, 2021
Study CompletionOct 8, 2021
TodayJul 2, 2026
Enrollment to primary: 12 monthsPosted 5.7 years ago

Interventions

ViSi devicedevice

Mobile patient monitoring system for vital signs.