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NCT05526768 · ClinicalTrials.gov registry record · NA

Evaluation of VITLS Compared to Traditional Inpatient Monitoring in Cardiac Shunt-Dependent Children

A NA study, sponsored by Baylor College of Medicine.

Completed
Registry status
NA
Development phase
27
Enrollment target

NCT05526768: Completed NA study, sponsored by Baylor College of Medicine.

NCT05526768 is a NA study that has completed, run by Baylor College of Medicine. The registered enrollment target is 27 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05526768, a NA study, has completed, sponsored by Baylor College of Medicine.

COMPLETED
Registry status
NA
Development phase
27 participants
Enrollment target

Study Summary

We are seeing how well a remote monitoring device that looks like a sticker placed on the chest, under the arm can monitor a child's vital signs including oxygen levels compared to the way that we usually get these measurements. The goal of this study is to see if the new sticker can be used for monitoring patients with cardiac shunt dependent heart conditions from home once they are discharged home. Participating children will be monitored for 6-72 hours with the new sticker in addition to his/her usual hospital monitors so the new sticker device can be compared to our hospital monitors.

Primary Outcome

Evaluate the VITLS device's ability to accurately measure pulse oximetry compared to conventional inpatient wall-connected methods in cardiac shunt-dependent children.

Interventions

  • DEVICE VITLS Device

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2022-10-26
Est. Completion 2023-05-10
Phase NA
Baylor College of Medicine

616 total trials

What the finished NCT05526768 record still lists

NCT05526768 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

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

NCT05526768 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05526768 about?

NCT05526768 is a clinical study titled "Evaluation of VITLS Compared to Traditional Inpatient Monitoring in Cardiac Shunt-Dependent Children". We are seeing how well a remote monitoring device that looks like a sticker placed on the chest, under the arm can monitor a child's vital signs including oxygen levels compared to the way that we usually get these measurements. The goal of this study is to see if the new sticker can be used for mon...

What is the current status of trial NCT05526768?

This trial is currently completed. It is a NA study. The enrollment target is 27 participants. The study started on 2022-10-26. Estimated completion is 2023-05-10.

What interventions are being tested in trial NCT05526768?

The interventions under investigation include: VITLS Device (DEVICE).

Who is sponsoring clinical trial NCT05526768?

This trial is sponsored by Baylor College of Medicine, which has 616 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05526768's enrollment target sits among peer trials

27 1708th of 2000 higher than 291 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05526768, the US trial registry maintained by the National Library of Medicine. NCT05526768 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.