CT-scan Airways Mensuration - Correlation to External Measurements
NCT ID: NCT02900807
Last Updated: 2018-08-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
134 participants
OBSERVATIONAL
2014-09-30
2017-03-23
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Which is the Best Bedside Test to Detect Endobronchial Intubation?
NCT01232166
Determining the Depth of Endotracheal Tube Insertion
NCT02158247
Compare a New Method and Formula as a Guide for the Intubation of a Left-sided Double-lumen Tube
NCT03545737
Measurement Of Endotracheal Tube Cuff Pressure In Emergency Department Patients
NCT01252173
A Comparison the Intubation of a Left Sided Double Lumen Tube and Uniblocker
NCT03392922
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* patient size between between 150 cm and 195 cm
Exclusion Criteria
* 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)
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Fondation Ophtalmologique Adolphe de Rothschild
NETWORK
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Guillaume Taylor, MD
Role: STUDY_DIRECTOR
Fondation OPH A de Rothschild
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Fondation Ophtalmologique Adolphe de Rothschild
Paris, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
GTR_2014_24
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.