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Uncuffed Endotracheal Tube vs. no Endotracheal Tube

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Enrolling

Conditions

Multiple Pulmonary Diseases

Treatments

Device: Endotracheal tube

Study type

Interventional

Funder types

Other

Identifiers

NCT06799455
PACCS-2024-33033

Details and patient eligibility

About

This is a comparison of uncuffed endotracheal tube (UCETT) vs. no endotracheal tube (ETT) in endobronchial ultrasound-transbronchial needle aspiration (EBUS-TBNA) procedure under moderate sedation in terms of procedure tolerance, duration of the procedure, desaturation, amount of sedation medication usage.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any patient that is scheduled for EBUS-TBNA procedure

Exclusion criteria

  • Those who are not safe to receive moderate sedation or flexible bronchoscopy

Trial design

Primary purpose

Health Services Research

Allocation

N/A

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

uncuffed endotracheal group
Experimental group
Treatment:
Device: Endotracheal tube
no endotracheal tube group/control
No Intervention group

Trial contacts and locations

1

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Central trial contact

Jamie Heisdorffer

Data sourced from clinicaltrials.gov

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