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NCT03093662 · ClinicalTrials.gov registry record · NA
Preoxygenation With Nasal Cannula and Noninvasive Positive Pressure Ventilation
A NA study of Hypoxia, sponsored by Brooke Army Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 37
- Enrollment target
- 1
- Study location
NCT03093662 is a NA study of Hypoxia that has completed, run by Brooke Army Medical Center. The registered enrollment target is 37 participants, below the 3,116-participant average among 39 other Hypoxia trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03093662, a NA study of Hypoxia, has completed, sponsored by Brooke Army Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 37 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a prospective randomized cross over study of healthy volunteers comparing end-tidal oxygen concentration among subjects undergoing continuous positive airway pressure ventilation via a noninvasive ventilation (NIV) mask with and without the addition of nasal cannulas.
Conditions Studied
Interventions
- DEVICE Ventilation with nasal cannula
- DEVICE Ventilation without nasal cannula
Study Locations (1)
Texas
- Brooke Army Medical Center - Fort Sam Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2017-03-02 |
| Est. Completion | 2017-03-09 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03093662
The ClinicalTrials.gov registry entry for NCT03093662 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,116-participant average among 39 other Hypoxia trials with a reported enrollment target (99% lower). The listed sponsor is Brooke Army Medical Center, which has 54 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Hypoxia appearing as the primary indexed condition, and to 2 interventions - of which Ventilation with nasal cannula is the first listed.
NCT03093662 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT03093662 about?
NCT03093662 is a clinical study titled "Preoxygenation With Nasal Cannula and Noninvasive Positive Pressure Ventilation". This is a prospective randomized cross over study of healthy volunteers comparing end-tidal oxygen concentration among subjects undergoing continuous positive airway pressure ventilation via a noninvasive ventilation (NIV) mask with and without the addition of nasal cannulas.
What is the current status of trial NCT03093662?
This trial is currently completed. It is a NA study. The enrollment target is 37 participants. The study started on 2017-03-02. Estimated completion is 2017-03-09.
What conditions does trial NCT03093662 study?
This clinical trial studies the following conditions: Hypoxia.
What interventions are being tested in trial NCT03093662?
The interventions under investigation include: Ventilation with nasal cannula (DEVICE), Ventilation without nasal cannula (DEVICE).
Who is sponsoring clinical trial NCT03093662?
This trial is sponsored by Brooke Army Medical Center, which has 54 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03093662 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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