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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02900807
Other study ID # GTR_2014_24
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2014
Est. completion date March 23, 2017

Study information

Verified date February 2018
Source Fondation Ophtalmologique Adolphe de Rothschild
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Oro-tracheal intubation is performed daily in anesthesia and in the ICU. When a patient is intubated, the endotracheal tube must be inserted into the trachea to the right depth. If the tube is not deep Inserted enough there is a risk of accidental extubation and trauma to the vocal cords by the balloon. If the tube is inserted too far there is a risk of selective intubation into the right or left mainstem bronchus, which can lead to contralateral lung atelectasis and hypoxemia.

The purpose of this study is to determine whether there is a correlation between the measurement of the airway of an adult population and criteria that would be easily accessible in daily clinical practice: the height of the patient and the size of their feet.


Recruitment information / eligibility

Status Completed
Enrollment 134
Est. completion date March 23, 2017
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patient scheduled for a CT-scan including the airways and the upper part of the chest at least until the carina

- patient size between between 150 cm and 195 cm

Exclusion Criteria:

- significant deformity of the cervical spine to accurately measure the size of patients (kyphoscoliosis...)

- impossibility of reliably know the size of the patient

- history of pharyngo-laryngeal surgery resulting in a significant deformity or a loss of anatomical landmarks incompatible with reliable measurements between dental arches and glottic plan (total laryngectomy...)

- history of lung surgery not allowing reliable location of the carina (pneumonectomy, double-lung transplant)

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Fondation Ophtalmologique Adolphe de Rothschild Paris

Sponsors (1)

Lead Sponsor Collaborator
Fondation Ophtalmologique Adolphe de Rothschild

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary size of the patients and/or size of their feet measured with a height chart and/or a pedometer Duration of the CT-scan : about 1 hour
Primary measurement of patients' airways Mensurations of airways measured on imaging (CT-scan) Duration of the CT-scan : about 1 hour
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