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NCT06578468 · ClinicalTrials.gov registry record · NA
End-Tidal Oxygen for Intubation in the Emergency Department
A NA study of Critical Illness and Respiratory Failure, sponsored by Sydney Local Health District.
- Recruiting
- Registry status
- NA
- Development phase
- 1,400
- Enrollment target
- 9
- Study locations
NCT06578468 is a NA study of Critical Illness and Respiratory Failure that is actively recruiting participants, run by Sydney Local Health District. The registered enrollment target is 1,400 participants, below the 3,123-participant average among 91 other Critical Illness trials with a reported enrollment target (55% lower). The trial reports 9 study locations across 5 states.
The verdict
NCT06578468, a NA study of Critical Illness and Respiratory Failure, is actively recruiting participants, sponsored by Sydney Local Health District.
- RECRUITING
- Registry status
- NA
- Development phase
- 1,400 participants
- Enrollment target
- 9
- Study locations
Study Summary
Rapid Sequence Intubation (RSI) is a high-risk procedure in the emergency department (ED). Patients are routinely preoxygenated (given supplemental oxygen) prior to RSI to prevent hypoxia during intubation. For many years anaesthetists have used end-tidal oxygen (ETO2) levels to guide the effectiveness of preoxygenation prior to intubation. The ETO2 gives an objective measurement of preoxygenation efficacy. This is currently not available in most EDs. This trial evaluates the use of ETO2 on the rate of hypoxia during intubation for patients in the ED.
Conditions Studied
Interventions
- DEVICE End-tidal oxygen monitor
Study Locations (9)
New South Wales
- Westmead Hospital - Sydney
- Royal Prince Alfred Hospital - Sydney
- Liverpool Hospital - Sydney
- Northern Beaches Hospital - Sydney
- Royal North Shore Hospital - Sydney
Minnesota
- Hennepin Medical Center - Minneapolis
New Mexico
- University of New Mexico Medical Center - Albuquerque
New York
- Lincoln Medical Center - The Bronx
Victoria
- The Alfred Hospital - Melbourne
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,400 participants |
| Start Date | 2024-08-05 |
| Est. Completion | 2025-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06578468
The ClinicalTrials.gov registry entry for NCT06578468 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 1,400 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,123-participant average among 91 other Critical Illness trials with a reported enrollment target (55% lower). The listed sponsor is Sydney Local Health District, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Critical Illness appearing as the primary indexed condition, and to 1 intervention - of which End-tidal oxygen monitor is the first listed.
NCT06578468 reports 9 study locations spanning 5 distinct geographic areas - top geographies include New South Wales, Minnesota, New Mexico.
Frequently Asked Questions
What is clinical trial NCT06578468 about?
NCT06578468 is a clinical study titled "End-Tidal Oxygen for Intubation in the Emergency Department". Rapid Sequence Intubation (RSI) is a high-risk procedure in the emergency department (ED). Patients are routinely preoxygenated (given supplemental oxygen) prior to RSI to prevent hypoxia during intubation. For many years anaesthetists have used end-tidal oxygen (ETO2) levels to guide the effectiven...
What is the current status of trial NCT06578468?
This trial is currently recruiting. It is a NA study. The enrollment target is 1,400 participants. The study started on 2024-08-05. Estimated completion is 2025-12-31.
What conditions does trial NCT06578468 study?
This clinical trial studies the following conditions: Critical Illness, Respiratory Failure, Hypoxia.
What interventions are being tested in trial NCT06578468?
The interventions under investigation include: End-tidal oxygen monitor (DEVICE).
Who is sponsoring clinical trial NCT06578468?
This trial is sponsored by Sydney Local Health District, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06578468 being conducted?
This trial has 9 study locations across Minnesota, New Mexico, New York, New South Wales, Victoria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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