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NCT04743206 · ClinicalTrials.gov registry record · NA
Airway Clearance for Pediatric and Adult Cystic Fibrosis Patients Using a Portable Intra-Pulmonary Percussion Device
A NA study, sponsored by University of Florida.
- Terminated
- Registry status
- NA
- Development phase
- 1
- Enrollment target
NCT04743206 is a NA study that was terminated before completion, run by University of Florida. The registered enrollment target is 1 participants.
The verdict
NCT04743206, a NA study, was terminated before completion, sponsored by University of Florida.
- TERMINATED
- Registry status
- NA
- Development phase
- 1 participants
- Enrollment target
Study Summary
This is a pilot study where the investigators aim to compare initial use of the standard airway clearance device (SACD), most commonly used being High frequency vest airway clearance system (VEST) with subsequent use of a Portable Intra-Pulmonary Percussion Device (PIAPD) in patients with cystic fibrosis (CF) ages 6 -21 years. The primary hypothesis is that there is no effect of PIAPD on Forced expiratory volume in 1 second (FEV1) 2 hours after use, there is no effect on perception of effort and efficacy for the PIAPD. If both are equally effective, the latter device provides an alternative that is both cheaper and portable.
Interventions
- DEVICE Standard Airway Clearance device
- DEVICE Portable Internal Airway Percussion device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1 participants |
| Start Date | 2021-05-18 |
| Est. Completion | 2021-08-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04743206
The ClinicalTrials.gov registry entry for NCT04743206 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Standard Airway Clearance device is the first listed.
NCT04743206 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04743206 about?
NCT04743206 is a clinical study titled "Airway Clearance for Pediatric and Adult Cystic Fibrosis Patients Using a Portable Intra-Pulmonary Percussion Device". This is a pilot study where the investigators aim to compare initial use of the standard airway clearance device (SACD), most commonly used being High frequency vest airway clearance system (VEST) with subsequent use of a Portable Intra-Pulmonary Percussion Device (PIAPD) in patients with cystic fib...
What is the current status of trial NCT04743206?
This trial is currently terminated. It is a NA study. The enrollment target is 1 participants. The study started on 2021-05-18. Estimated completion is 2021-08-01.
What interventions are being tested in trial NCT04743206?
The interventions under investigation include: Standard Airway Clearance device (DEVICE), Portable Internal Airway Percussion device (DEVICE).
Who is sponsoring clinical trial NCT04743206?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
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