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NCT06406725 · ClinicalTrials.gov registry record
Detection of Vocal Fold Motion Impairment on Noninvasive Positive Pressure
A clinical trial of Vocal Cord Dysfunction and Vocal Cord Paralysis, sponsored by Northwell Health.
- Recruiting
- Registry status
- 50
- Enrollment target
- 1
- Study location
NCT06406725: Recruiting study of Vocal Cord Dysfunction and Vocal Cord Paralysis, sponsored by Northwell Health.
NCT06406725 is a study of Vocal Cord Dysfunction and Vocal Cord Paralysis that is actively recruiting participants, run by Northwell Health. The registered enrollment target is 50 participants, roughly in line with the 52-participant average among 3 other Vocal Cord Dysfunction trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06406725, a study of Vocal Cord Dysfunction and Vocal Cord Paralysis, is actively recruiting participants, sponsored by Northwell Health.
- RECRUITING
- Registry status
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this prospective, observational study is to evaluate for the presence of vocal fold motion impairment (VFMI) in the children admitted to the pediatric intensive care unit on noninvasive positive pressure ventilation (NIV PPV). Participants will have two ultrasounds of their vocal folds performed, once while on NIV PPV and once after weaned off of the NIV PPV. This results of these scans will be reviewed against one another and against the gold standard, fiberoptic nasolaryngoscopy (FNL). The main question this study aims to answer is: Can POCUS be used to reliably detect VFMI while pediatric patients on supported with NIV PPV?
Primary Outcome
Our primary outcome measure will be the detection of vocal fold motion impairment on patients as detected by laryngeal point-of-care ultrasound while on NIV PPV.
Conditions Studied
Interventions
- DIAGNOSTIC_TEST Point-of-Care Ultrasound of the Airway
Study Locations (1)
New York
- Cohen Children's Medical Center - Queens
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2024-03-30 |
| Est. Completion | 2026-05-30 |
What NCT06406725 shows while recruiting
NCT06406725 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target, roughly in line with the 52-participant average among 3 other Vocal Cord Dysfunction trials with a reported enrollment target.
The record links to 5 conditions, with Vocal Cord Dysfunction appearing as the primary indexed condition, and to 1 intervention - of which Point-of-Care Ultrasound of the Airway is the first listed.
NCT06406725 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT06406725 about?
NCT06406725 is a clinical study titled "Detection of Vocal Fold Motion Impairment on Noninvasive Positive Pressure". The goal of this prospective, observational study is to evaluate for the presence of vocal fold motion impairment (VFMI) in the children admitted to the pediatric intensive care unit on noninvasive positive pressure ventilation (NIV PPV). Participants will have two ultrasounds of their vocal folds p...
What is the current status of trial NCT06406725?
This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2024-03-30. Estimated completion is 2026-05-30.
What conditions does trial NCT06406725 study?
This clinical trial studies the following conditions: Vocal Cord Dysfunction, Vocal Cord Paralysis, Vocal Cord Paresis, Recurrent Laryngeal Nerve Palsy, Recurrent Laryngeal Nerve Injuries.
What interventions are being tested in trial NCT06406725?
The interventions under investigation include: Point-of-Care Ultrasound of the Airway (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT06406725?
This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06406725 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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