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NCT02029300 · ClinicalTrials.gov registry record · NA
A Comparison of Nasal Versus Oral Fiberoptic Intubation in Children
A NA study, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT02029300 is a NA study that has completed, run by Ann & Robert H Lurie Children's Hospital of Chicago. The registered enrollment target is 100 participants.
The verdict
NCT02029300, a NA study, has completed, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study Summary
There are two routes in which a fiberoptic intubation can be performed - oral and nasal. In general, nasal intubation by any conventional method may be the preferred choice for certain procedures such as intra-oral surgeries, or for anatomical reasons such as limited mouth opening. If nasal intubation is not indicated or preferred, then oral intubation is usually performed. This study is looking to explore whether or not the nasal route significantly improves the ease and time for successful fiberoptic intubation compared to the oral route in children less than or equal to 2 years of age. This study will also examine if operator experience influence time to tracheal intubation with either route? The investigators hypothesize that the nasal route of fiberoptic intubation will be faster than the oral route, for both the trainee and the expert, and that there will be minimal differences between experts and trainees with nasal fiberoptic intubation.
Interventions
- OTHER Fiberoptic Intubation through the nasal route
- OTHER Fiberoptic intubation through the oral route
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2013-11 |
| Est. Completion | 2014-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02029300
The ClinicalTrials.gov registry entry for NCT02029300 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Fiberoptic Intubation through the nasal route is the first listed.
NCT02029300 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02029300 about?
NCT02029300 is a clinical study titled "A Comparison of Nasal Versus Oral Fiberoptic Intubation in Children". There are two routes in which a fiberoptic intubation can be performed - oral and nasal. In general, nasal intubation by any conventional method may be the preferred choice for certain procedures such as intra-oral surgeries, or for anatomical reasons such as limited mouth opening. If nasal intubati...
What is the current status of trial NCT02029300?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2013-11. Estimated completion is 2014-03.
What interventions are being tested in trial NCT02029300?
The interventions under investigation include: Fiberoptic Intubation through the nasal route (OTHER), Fiberoptic intubation through the oral route (OTHER).
Who is sponsoring clinical trial NCT02029300?
This trial is sponsored by Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total clinical trials registered on ClinicalTrials.gov.
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