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Comparison of Intubation Conditions of the Articulating Stylet and Intubating Stylet Guided Videolaryngoscopy

Comparison of Intubation Conditions of the Articulating Stylet and Intubating Stylet Guided Videolaryngoscopy in Patients With Difficult Airway

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02805569
Enrollment
49
Registered
2016-06-20
Start date
2016-06-30
Completion date
2018-02-28
Last updated
2018-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Difficult Intubation

Keywords

videolaryngoscope, intubation stylet, articulating stylet, difficult airway

Brief summary

Indirect videolaryngoscopes provide an improved view of the glottis. Unfortunately enhanced video blade angulation leads to difficulty in passage of the endotracheal tube (ETT) towards the larynx around the steep blade angulation despite adequate visualization of the glottis. Pre-shaping the ETT with the rigit malleable stylet is recommended. The investigators hypothesized that using articulating stylet (AS) would enhance first attempt intubation, shorten the intubation time, reduce the possibility of the soft tissue trauma compared to conventional intubation stylet (IS) in patients with difficult airway .

Detailed description

Patients with known airway difficulty (anticipated difficult airway (ADA) score \>6) will be included to the study. All patients will receive general anesthesia for a variety of elective surgical procedure. Tracheal intubation will be performed by senior anesthesiologist. Patients will be intubated using AS-videolaryngoscope (n= 24) or IS-videolaryngoscope (n=24) randomly. Patients demographic details (age 18-65 yr, body mass index, ASA phisical status), ADA scores, Cormack-Lehane scores, intubation difficulty scores, intubation attempts, intubation time, hemodynamic variables, sore throat, anesthesiologists satisfaction will be recorded.

Interventions

DEVICEarticulating stylet

patient who intubated with articulating stylet

DEVICEconventional stylet

patient who intubated with conventional stylet

Sponsors

Diskapi Teaching and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* ASA 1-2 physical status (Anticipated difficult airway) ADA scores \>6 Elective surgery

Exclusion criteria

* ASA 3-4 physical status Immobilizedcervical spine

Design outcomes

Primary

MeasureTime frameDescription
intibation timeThrough intubation completion, an avarage of 5 minutesTotal intubation time (second)

Secondary

MeasureTime frameDescription
tracheal intubation attemptsThrough intubation completion, an avarage of 5 minutesnumber of intubation attempts

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026