University Clinical Hospital of Santiago de Compostela
Santiago de Compostela, A Coruña, 15866, Spain
Location status: Recruiting
Location contact
Manuel Taboada Muñiz, Ph.D.
CONTACT
María Teresa Cabaleiro Ocampo
CONTACT
NCT Number: NCT05429125
Although VLs improve glottic visualization, on many occasions it may not be accompanied by intubation at the first attempt, because the endotracheal tube has to pass a sharp angle to enter the trachea. To avoid this limitation, a new flexible tip bougie is designed to flexibly navigate the distal tip and help facilitate precise insertion of the endotracheal tube in the trachea. The flexible tip bougie has an integrated slider along the surface which moves the tip anterior and posterior while the pre-curved distal portion of shaft allows the angulation to provide anterior flexion. This new flexible tip bougie could be used as a rescue when first intubation failure using the videolaryngoscopy, or as a first option to improve the percentage of patients intubated at the first attempt.
Interested in participating?
Request Info18 year–90 year
All sexes
Interventional
Not applicable
Santiago de Compostela, A Coruña, 15866, Spain
Location status: Recruiting
Manuel Taboada Muñiz, Ph.D.
CONTACT
María Teresa Cabaleiro Ocampo
CONTACT
The purpose of this prospective randomized study is to compare successful intubation on the first attempt with the new flexible tip bougie versus endotracheal tube with stylet during awake intubation with videolaryngoscopy in patients with anticipated difficult airway.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients randomised to Endotracheal Tube with Stylet will be intubated with a Videolaryngoscopy and with an endotracheal tube + stylet.
Patients randomised to Flexible Tip Bougie will be intubated with a Videolaryngoscopy and with a Flexible Tip Bougie.
Time frame: During intubation
To compare the difference in the first attempt intubation success rate (percentage) with the two differents devices compared.
Time frame: During intubation
To compare the difference overall intubation success rate (percentage) with the two differents devices compared.
Time frame: Participants will be followed from the beginning of the intervention to 30 minutes after the intervention
To compare the difference in complications (percentage) with the two different devices compared:
Hypoxemia (SpO2) < 90 %, Hypoxemia severe (SpO2) < 80 %, Hypotension defined as systolic blood pressure less than 80 mm Hg, Severe hypotension defined as systolic blood pressure less than 65 mm Hg, Cardiac arrest, death during intubation, Moderate or difficult intubation, oesophageal intubation, pulmonary aspiration, dental injuries.
Time frame: During intubation
Operator-assessed subjective difficulty of intubation by means of a special analogue numerical scale from 0 to 10, where 0=no subjective difficulty and 10=maximal subjective difficulty
Time frame: During intubation
Modified Cormack-Lehane grade of glottic view:
I: full view of the glottis IIa: partial view of the glottis IIb: arytenoid or posterior part of the vocal cords just visible III: only epiglottis visible IV: neither glottis nor epiglottis visible
Time frame: During intubation
Need for additional airway equipment
Time frame: During intubation
Number of intubation attempts
Contact information is provided by the study sponsor or research team.
Manuel Taboada Muñiz, Ph.D.
CONTACT
Manuel Taboada Muñiz, Ph.D.
CONTACT
Hospital Clinico Universitario de Santiago
Other
A Randomized Comparison Between the Flexible Tip Bougie vs Tube With Stylet for First-attempt Intubation Success With the C-MAC Videolaryngoscopy in Patients With Anticipated Difficult Airway
Acronym: VIFLEXTIPOR
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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