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NCT06737432 · ClinicalTrials.gov registry record · NA
Respiratory Knowledge Portal Computer and Phone Application to Improve Quality of Mechanical Ventilation by Reducing the Number of Ventilator Associated Events, Injury Created by the Ventilator and Unsafe Setting of Alarms.
A NA study of Respiratory Failure and ARDS, sponsored by The University of Texas Medical Branch, Galveston.
- Recruiting
- Registry status
- NA
- Development phase
- 800
- Enrollment target
- 1
- Study location
NCT06737432: Recruiting NA study of Respiratory Failure and ARDS, sponsored by The University of Texas Medical Branch, Galveston.
NCT06737432 is a NA study of Respiratory Failure and ARDS that is actively recruiting participants, run by The University of Texas Medical Branch, Galveston. The registered enrollment target is 800 participants, below the 4,504-participant average among 40 other Respiratory Failure trials with a reported enrollment target (82% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06737432, a NA study of Respiratory Failure and ARDS, is actively recruiting participants, sponsored by The University of Texas Medical Branch, Galveston.
- RECRUITING
- Registry status
- NA
- Development phase
- 800 participants
- Enrollment target
- 1
- Study location
Study Summary
Ventilator associated events (VAE) is a quality metric defined by 48 hours of stability followed by 48 hours of escalation of ventilator settings within the ICU. VAE have been associated with poor outcomes and increases the cost of care, yet is not easy to avoid. Operationalizing all the standards of care known to improve outcomes of those requiring mechanical ventilation in the critical care environment requires a comprehensive approach. ICU teams are encouraged to follow best practice protocols to help liberate and prevent VAEs. Yet, compliance with protocols in most ICUs is suboptimal for multiple reasons. With the advent of computerized mechanical ventilators capable of streaming data from breath to breath and biomedical integration systems (BMDI) such as Capsule (UTMB's BMDI system), software systems have been developed to help identify variances in the standard of care. Automation in near real-time ventilator data feedback has been shown to reduce the incidences of VAEs. This quality improvement project will leverage Vyaire's Respiratory Knowledge Portal (RKP) to collect and store meaningful data regarding ventilator-associated events (VAE), alarm policy compliance, ventilator weaning, and lung protective analytics. Goals: 1. To collect quality metrics utilizing RKP from patients requiring mechanical ventilation over a 3-4-month period for a retrospective baseline analysis. 2. Provide the RKP tool to the ICU team to determine if the use of RKP's webportal and Messenger Zebra phone app improves quality of mechanical ventilation and outcomes. 3. To determine a return on investment (ROI) for a software system like RKP.
Conditions Studied
Interventions
- OTHER RKP Monitoring Software
Study Locations (1)
Texas
- University of Texas Medical Branch - Galveston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 800 participants |
| Start Date | 2024-06-01 |
| Est. Completion | 2026-05 |
| Phase | NA |
What NCT06737432 shows while recruiting
NCT06737432 is an interventional study that assigns participants to a tested intervention. The registered 800 participants enrollment target is mid-sized for trials with a published cap, below the 4,504-participant average among 40 other Respiratory Failure trials with a reported enrollment target (82% lower).
The record links to 7 conditions, with Respiratory Failure appearing as the primary indexed condition, and to 1 intervention - of which RKP Monitoring Software is the first listed.
NCT06737432 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT06737432 about?
NCT06737432 is a clinical study titled "Respiratory Knowledge Portal Computer and Phone Application to Improve Quality of Mechanical Ventilation by Reducing the Number of Ventilator Associated Events, Injury Created by the Ventilator and Unsafe Setting of Alarms.". Ventilator associated events (VAE) is a quality metric defined by 48 hours of stability followed by 48 hours of escalation of ventilator settings within the ICU. VAE have been associated with poor outcomes and increases the cost of care, yet is not easy to avoid. Operationalizing all the standards o...
What is the current status of trial NCT06737432?
This trial is currently recruiting. It is a NA study. The enrollment target is 800 participants. The study started on 2024-06-01. Estimated completion is 2026-05.
What conditions does trial NCT06737432 study?
This clinical trial studies the following conditions: Respiratory Failure, ARDS, Mechanical Ventilation, Quality Improvement, Ventilation.
What interventions are being tested in trial NCT06737432?
The interventions under investigation include: RKP Monitoring Software (OTHER).
Who is sponsoring clinical trial NCT06737432?
This trial is sponsored by The University of Texas Medical Branch, Galveston, which has 203 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06737432 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT06737432's enrollment target sits among peer trials
800 8th of 40 higher than 33 of 40 other Respiratory Failure trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Respiratory Failure 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.
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