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NCT01285804 · ClinicalTrials.gov registry record · NA
Impact of Using a Cuffed Endotracheal Tube on Limiting the Risk of Airway Fire
A NA study of Tonsillectomy and Adenoidectomy, sponsored by Nationwide Children's Hospital.
- Completed
- Registry status
- NA
- Development phase
- 200
- Enrollment target
- 1
- Study location
NCT01285804: Completed NA study of Tonsillectomy and Adenoidectomy, sponsored by Nationwide Children's Hospital.
NCT01285804 is a NA study of Tonsillectomy and Adenoidectomy that has completed, run by Nationwide Children's Hospital. The registered enrollment target is 200 participants, below the 1,759-participant average among 6 other Tonsillectomy trials with a reported enrollment target (89% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01285804, a NA study of Tonsillectomy and Adenoidectomy, has completed, sponsored by Nationwide Children's Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to evaluate the impact of using a cuffed endotracheal tube (ETT) on the oxygen concentration in the oropharynx during adenoidectomy, tonsillectomy, or adenotonsillectomy. The study hypothesis is that inflation of the cuff on the ETT will eliminate contamination of the oropharynx with the inspired anesthetic gases and decrease the oxygen concentration in the oropharynx.
Primary Outcome
The oxygen and sevoflurane (anesthetic agent) concentration of the oropharynx would be measured during positive pressure ventilation immediately after intubation and then 4-5 mins. after anesthetic induction when the patient resumes spontaneous ventilation.
Conditions Studied
Interventions
- OTHER Cuffed ETT
- OTHER Uncuffed ETT
Study Locations (1)
Ohio
- Nationwide Children's Hospital - Columbus
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2011-01 |
| Est. Completion | 2011-11 |
| Phase | NA |
What the finished NCT01285804 record still lists
NCT01285804 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 1,759-participant average among 6 other Tonsillectomy trials with a reported enrollment target (89% lower).
The record links to 3 conditions, with Tonsillectomy appearing as the primary indexed condition, and to 2 interventions - of which Cuffed ETT is the first listed.
NCT01285804 reports a single indexed study location in Ohio.
Frequently Asked Questions
What is clinical trial NCT01285804 about?
NCT01285804 is a clinical study titled "Impact of Using a Cuffed Endotracheal Tube on Limiting the Risk of Airway Fire". The purpose of this study is to evaluate the impact of using a cuffed endotracheal tube (ETT) on the oxygen concentration in the oropharynx during adenoidectomy, tonsillectomy, or adenotonsillectomy. The study hypothesis is that inflation of the cuff on the ETT will eliminate contamination of the or...
What is the current status of trial NCT01285804?
This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2011-01. Estimated completion is 2011-11.
What conditions does trial NCT01285804 study?
This clinical trial studies the following conditions: Tonsillectomy, Adenoidectomy, Adenotonsillectomy.
What interventions are being tested in trial NCT01285804?
The interventions under investigation include: Cuffed ETT (OTHER), Uncuffed ETT (OTHER).
Who is sponsoring clinical trial NCT01285804?
This trial is sponsored by Nationwide Children's Hospital, which has 188 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01285804 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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