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NCT05245747 · ClinicalTrials.gov registry record
Vitls Feasibility Physiologic Monitoring
A clinical trial of Pediatrics and Remote Monitoring, sponsored by Children's Mercy Hospital Kansas City.
- Completed
- Registry status
- 20
- Enrollment target
- 1
- Study location
NCT05245747 is a study of Pediatrics and Remote Monitoring that has completed, run by Children's Mercy Hospital Kansas City. The registered enrollment target is 20 participants, below the 1,341-participant average among 15 other Pediatrics trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05245747, a study of Pediatrics and Remote Monitoring, has completed, sponsored by Children's Mercy Hospital Kansas City.
- COMPLETED
- Registry status
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
A single site, cross-sectional, feasibility study will be used to evaluate the feasibility of the collection of physiologic data related to the use of the Vitls Platform in the pediatric (\< 2 year of age) congenital heart and general surgery populations in the hospital setting that is using 24 hour a day monitoring for routine care over a 48-hour period. A short questionnaire will be sent electronically for the parent-child dyad feedback after the participating child has worn the device. No data will be available at the time of placement for the Healthcare team and will not replace any routine/standard of care monitoring already in place for this complex population.
Conditions Studied
Interventions
- DEVICE Vitls Tego Device
Study Locations (1)
Missouri
- Children's Mercy Kansas City - Kansas City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2022-02-28 |
| Est. Completion | 2023-05-16 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05245747
The ClinicalTrials.gov registry entry for NCT05245747 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,341-participant average among 15 other Pediatrics trials with a reported enrollment target (99% lower). The listed sponsor is Children's Mercy Hospital Kansas City, which has 184 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Pediatrics appearing as the primary indexed condition, and to 1 intervention - of which Vitls Tego Device is the first listed.
NCT05245747 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.
Frequently Asked Questions
What is clinical trial NCT05245747 about?
NCT05245747 is a clinical study titled "Vitls Feasibility Physiologic Monitoring". A single site, cross-sectional, feasibility study will be used to evaluate the feasibility of the collection of physiologic data related to the use of the Vitls Platform in the pediatric (\< 2 year of age) congenital heart and general surgery populations in the hospital setting that is using 24 hour...
What is the current status of trial NCT05245747?
This trial is currently completed. The enrollment target is 20 participants. The study started on 2022-02-28. Estimated completion is 2023-05-16.
What conditions does trial NCT05245747 study?
This clinical trial studies the following conditions: Pediatrics, Remote Monitoring, Vital Signs.
What interventions are being tested in trial NCT05245747?
The interventions under investigation include: Vitls Tego Device (DEVICE).
Who is sponsoring clinical trial NCT05245747?
This trial is sponsored by Children's Mercy Hospital Kansas City, which has 184 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05245747 being conducted?
This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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