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NCT01150838 · ClinicalTrials.gov registry record · Phase 4
Propofol for Pediatric Tracheal Intubation With Deep Anesthesia During Sevoflurane Induction
A Phase 4 study, sponsored by University of Virginia.
- Completed
- Registry status
- Phase 4
- Development phase
- 106
- Enrollment target
NCT01150838 is a Phase 4 study that has completed, run by University of Virginia. The registered enrollment target is 106 participants.
The verdict
NCT01150838, a Phase 4 study, has completed, sponsored by University of Virginia.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 106 participants
- Enrollment target
Study Summary
The purpose of this study is to determine the amount of propofol required to achieve 50% of patients obtaining a perfect ("excellent") intubation score of 5 on the Steyn modification of the Helbo-Hansen Intubation Score, when placing a tracheal tube in children 1-6 years and 6-12 years (division of age groups at 6th birthday) of age, under a specific induction and ventilation sequence as specified in this study design.
Interventions
- DRUG propofol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 106 participants |
| Start Date | 2008-07 |
| Est. Completion | 2010-06 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01150838
The ClinicalTrials.gov registry entry for NCT01150838 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 106 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Virginia, which has 449 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which propofol is the first listed.
NCT01150838 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01150838 about?
NCT01150838 is a clinical study titled "Propofol for Pediatric Tracheal Intubation With Deep Anesthesia During Sevoflurane Induction". The purpose of this study is to determine the amount of propofol required to achieve 50% of patients obtaining a perfect ("excellent") intubation score of 5 on the Steyn modification of the Helbo-Hansen Intubation Score, when placing a tracheal tube in children 1-6 years and 6-12 years (division of ...
What is the current status of trial NCT01150838?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 106 participants. The study started on 2008-07. Estimated completion is 2010-06.
What interventions are being tested in trial NCT01150838?
The interventions under investigation include: propofol (DRUG).
Who is sponsoring clinical trial NCT01150838?
This trial is sponsored by University of Virginia, which has 449 total clinical trials registered on ClinicalTrials.gov.
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