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NCT02003287 · ClinicalTrials.gov registry record · NA
Comparing FEES to VFSS in Diagnosing Laryngeal Penetration and Aspiration in Infants in the NICU
A NA study, sponsored by Baylor Research Institute.
- Completed
- Registry status
- NA
- Development phase
- 25
- Enrollment target
NCT02003287 is a NA study that has completed, run by Baylor Research Institute. The registered enrollment target is 25 participants.
The verdict
NCT02003287, a NA study, has completed, sponsored by Baylor Research Institute.
- COMPLETED
- Registry status
- NA
- Development phase
- 25 participants
- Enrollment target
Study Summary
The main purpose of the study is to determine whether the Fiberoptic Endoscopic Evaluation of Swallowing (FEES) is effective in detecting laryngeal penetration and tracheal aspiration when compared with the Videofluoroscopic Swallowing Study (VFSS) in bottle-feeding infants in the NICU. A secondary objective is to determine whether FEES can be used to detect laryngeal penetration and tracheal aspiration in breastfeeding NICU infants.
Interventions
- OTHER VFSS
- OTHER FEES
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2013-11 |
| Est. Completion | 2014-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02003287
The ClinicalTrials.gov registry entry for NCT02003287 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baylor Research Institute, which has 180 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which VFSS is the first listed.
NCT02003287 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02003287 about?
NCT02003287 is a clinical study titled "Comparing FEES to VFSS in Diagnosing Laryngeal Penetration and Aspiration in Infants in the NICU". The main purpose of the study is to determine whether the Fiberoptic Endoscopic Evaluation of Swallowing (FEES) is effective in detecting laryngeal penetration and tracheal aspiration when compared with the Videofluoroscopic Swallowing Study (VFSS) in bottle-feeding infants in the NICU. A secondary ...
What is the current status of trial NCT02003287?
This trial is currently completed. It is a NA study. The enrollment target is 25 participants. The study started on 2013-11. Estimated completion is 2014-10.
What interventions are being tested in trial NCT02003287?
The interventions under investigation include: VFSS (OTHER), FEES (OTHER).
Who is sponsoring clinical trial NCT02003287?
This trial is sponsored by Baylor Research Institute, which has 180 total clinical trials registered on ClinicalTrials.gov.
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