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Ultrasound for Double Lumen Endotracheal Tube

4

424 General Military Hospital

Status

Terminated

Conditions

Lung Ultrasound

Treatments

Device: Determination of tube position by ultrasound.
Other: Determination of tube position by auscultation.

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The patients will be allocated to 2 groups: the ultrasound group and the clinical group. The correct position of the double lumen tube will be determined by ultrasound (Sonoscape S6®) for the patients of the one group (group U) and by clinical examination for the patients of the other group (group C). The correct placement will be verified by bronchoscopy (Pentax®). The two methods will be compared in terms of sensitivity and specificity. The main purpose of the study is to determine if the ultrasound can be used for determination of the correct placement of the left sided double lumen endotracheal tube

Enrollment

5 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Surgery requiring placement of double-lumen endotracheal tube.
  • ASA 1-3

Exclusion criteria

  • History of difficult or impossible intubation.
  • Clinical findings of possible difficult intubation according to the standard preoperative airway assessment.
  • Impossible placement of a double lumen tube

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

5 participants in 2 patient groups

Ultrasound
Experimental group
Description:
Determination of correct placement of the double lumen tube by lung ultrasound.
Treatment:
Device: Determination of tube position by ultrasound.
Clinical
Active Comparator group
Description:
Determination of correct placement of the double lumen tube by clinical examination.
Treatment:
Other: Determination of tube position by auscultation.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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