Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02202798 · ClinicalTrials.gov registry record
New Devices to Measure the Intracuff Pressure
A clinical trial of Patients Intubated With a Cuffed Endotracheal Tube, sponsored by Joseph D. Tobias.
- Completed
- Registry status
- 400
- Enrollment target
- 1
- Study location
NCT02202798 is a study of Patients Intubated With a Cuffed Endotracheal Tube that has completed, run by Joseph D. Tobias. The registered enrollment target is 400 participants. The trial reports 1 study location across 1 state.
The verdict
NCT02202798, a study of Patients Intubated With a Cuffed Endotracheal Tube, has completed, sponsored by Joseph D. Tobias.
- COMPLETED
- Registry status
- 400 participants
- Enrollment target
- 1
- Study location
Study Summary
Over the past 5 years, there has been a change in clinical practice with the use of cuffed instead of uncuffed endotracheal tubes in infants and children. Two manufacturing companies have recently introduced syringe-like devices to the market which allow the measurement of the intracuff pressure. This study proposes to prospectively compare the intracuff pressure from these devices with the gold standard technique (manometer).
Conditions Studied
Interventions
- DEVICE Syringe device
Study Locations (1)
Ohio
- Nationwide Children's Hospital - Columbus
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2013-11 |
| Est. Completion | 2014-08 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02202798
The ClinicalTrials.gov registry entry for NCT02202798 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Joseph D. Tobias, which has 21 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Patients Intubated With a Cuffed Endotracheal Tube appearing as the primary indexed condition, and to 1 intervention - of which Syringe device is the first listed.
NCT02202798 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.
Frequently Asked Questions
What is clinical trial NCT02202798 about?
NCT02202798 is a clinical study titled "New Devices to Measure the Intracuff Pressure". Over the past 5 years, there has been a change in clinical practice with the use of cuffed instead of uncuffed endotracheal tubes in infants and children. Two manufacturing companies have recently introduced syringe-like devices to the market which allow the measurement of the intracuff pressure. Th...
What is the current status of trial NCT02202798?
This trial is currently completed. The enrollment target is 400 participants. The study started on 2013-11. Estimated completion is 2014-08.
What conditions does trial NCT02202798 study?
This clinical trial studies the following conditions: Patients Intubated With a Cuffed Endotracheal Tube.
What interventions are being tested in trial NCT02202798?
The interventions under investigation include: Syringe device (DEVICE).
Who is sponsoring clinical trial NCT02202798?
This trial is sponsored by Joseph D. Tobias, which has 21 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02202798 being conducted?
This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.