MedTrace Logo

Ultrasound-detectable Endotracheal Tube: a Feasibility Study

NCT05941013 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2026-02-05

No results posted yet for this study

Summary

The researchers are studying whether special features make it easier to see if the breathing tube is in the correct place. It is hoped that the investigational device will enable more accurate placement (depth and trachea vs. esophagus).

Conditions

  • Cardiac Catheterization
  • Endotracheal Tube

Interventions

DEVICE

Ultrasound detectable cuffed endotracheal tube (USD-ETT)

Intubation with a novel ultrasound-detectable endotracheal tube

Sponsors & Collaborators

  • John R. Charpie

    lead OTHER

Principal Investigators

  • John Charpie, MD, PhD · University of Michigan

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
6 Months
Max Age
42 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-15
Primary Completion
2027-03-31
Completion
2027-04-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05941013 on ClinicalTrials.gov