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NCT04574908 · ClinicalTrials.gov registry record · NA

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

A NA study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
NA
Development phase
879
Enrollment target

NCT04574908 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 879 participants.

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The verdict

NCT04574908, a NA study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
NA
Development phase
879 participants
Enrollment target

Study 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.

Interventions

  • DEVICE ViSi device

Trial Details

FieldValue
Enrollment Target 879 participants
Start Date 2020-10-07
Est. Completion 2021-10-08
Phase NA

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT04574908

The ClinicalTrials.gov registry entry for NCT04574908 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 879 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which ViSi device is the first listed.

NCT04574908 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04574908 about?

NCT04574908 is a clinical study titled "A Pilot Trial of Continuous Portable Postoperative Hemodynamic And Saturation Monitoring On Hospital Wards". 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 ...

What is the current status of trial NCT04574908?

This trial is currently completed. It is a NA study. The enrollment target is 879 participants. The study started on 2020-10-07. Estimated completion is 2021-10-08.

What interventions are being tested in trial NCT04574908?

The interventions under investigation include: ViSi device (DEVICE).

Who is sponsoring clinical trial NCT04574908?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.