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Intra-op POCUS for Identification of Endotracheal Tube Position in the Pediatric Population
NCT03031548 · View on ClinicalTrials.gov ↗
Study Summary
Chest X-ray and/or fluoroscopy is not routinely used in the OR to confirm endotracheal tube (ETT) placement by anesthesiologists. Multiple studies have shown that \~19% of all intubations result in inappropriate ETT placement. An adult study has shown that ultrasound point-of-care is superior to auscultation in determining the location of ETT. This study aims to determine if point-of-care is useful in determining ETT position in children.
Conditions Studied
Interventions
- DEVICE Point-of-care ultrasound exam
- RADIATION Reposition ETT
Study Locations (2)
California
- Loma Linda University Health — Loma Linda
- Loma Linda University Department of Anesthesiology — Loma Linda
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2017-02-16 |
| Est. Completion | 2018-06-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03031548
The ClinicalTrials.gov registry entry for NCT03031548 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Loma Linda University, which has 191 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Endotracheal Tube Wrongly Placed During Anesthetic Procedure appearing as the primary indexed condition, and to 2 interventions — of which Point-of-care ultrasound exam is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03031548 reports 2 study locations spanning 1 distinct geographic area — top geographies include California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03031548 about?
NCT03031548 is a clinical study titled "Intra-op POCUS for Identification of Endotracheal Tube Position in the Pediatric Population". Chest X-ray and/or fluoroscopy is not routinely used in the OR to confirm endotracheal tube (ETT) placement by anesthesiologists. Multiple studies have shown that \~19% of all intubations result in inappropriate ETT placement. An adult study has shown that ultrasound point-of-care is superior to aus...
What is the current status of trial NCT03031548?
This trial is currently completed. The enrollment target is 50 participants. The study started on 2017-02-16. Estimated completion is 2018-06-30.
What conditions does trial NCT03031548 study?
This clinical trial studies the following conditions: Endotracheal Tube Wrongly Placed During Anesthetic Procedure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03031548?
The interventions under investigation include: Point-of-care ultrasound exam (DEVICE), Reposition ETT (RADIATION). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03031548?
This trial is sponsored by Loma Linda University, which has 191 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03031548 being conducted?
This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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