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Impact of Covid-19 Aerosol Box On Intubation Success Rate

Impact of Covid-19 Aerosol Box On Intubation Success Rate and Intubation Time

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06042829
Enrollment
60
Registered
2023-09-21
Start date
2020-11-23
Completion date
2021-11-22
Last updated
2023-09-21

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

Conditions

Intubation; Difficult or Failed

Brief summary

The safety of novel medical device must be assessed before being implemented into clinical practice. In the case of aerosol box, one of the safety features concerned includes its impact on intubation and how it affect the probability of efficient intubation in order to avoid risk of hypoxia to patient. As the barrier box is newly invented, there have been limited studies published. This study aims to compare intubation success rate between intubation with and without aerosol box in real patients, which will determine the chances of efficient intubation and reflect the safety features of the aerosol box.

Detailed description

General Objective To determine whether intubation performed using aerosol box will have a lower chance of success as compared to intubation without using the box. Specific Objectives 1. To determine whether intubation with aerosol box will require more time for successful intubation as compared to intubation without the box. 2. To compare the ease of intubation and determine whether intubation using aerosol box will require additional airway manipulation as compared to intubation without using the box.

Interventions

DEVICEIntubation using aerosol box

Intubation time and ease of intubation using aerosol box

DEVICEIntubation without aerosol box

Intubation time and ease of intubation without aerosol box

Sponsors

Universiti Kebangsaan Malaysia Medical Centre
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age \> 18 years old 2. American Society of Anesthesiologist (ASA) I or II patients 3. Tested negative for COVID-19 prior to surgery 4. Patient scheduled for elective surgery under general anaesthesia

Exclusion criteria

1. Claustrophobia 2. Difficult airway features 3. Body mass index (BMI) of more than 35 kg/m2 4. Body habitus not physically fit into the aerosol box.

Design outcomes

Primary

MeasureTime frameDescription
Tracheal intubation time1 yearTime taken from the laryngoscope blade passes through front incisors, followed by endotracheal intubation being inserted into trachea, and until the first upstroke of the capnograph trace visible as proof of successful tracheal intubation (the measurement is measured in seconds)

Secondary

MeasureTime frameDescription
Ease of tracheal intubation1 yearBased on scale of tracheal intubation difficulty. The scale is called Intubation Difficulty Scale. Intubation difficulty scale is a numerical score of total intubation difficulty and is based on seven parameters known to be associated with difficult intubation. The seven parameters are number of attempts, number of intubators, number of alternative techniques, Cormack-Lehane laryngoscopy grades, requirement of lifting force of laryngoscopy, application of laryngeal pressure, and mobility of vocal cords. The score will be summed. The degree of difficulty will be categorized into easy (IDS score of 0), slight difficulty (IDS of 1-4) and moderate to major difficulty (IDS of 5 and more) according to the total score. The higher score is associated with a higher prevalence of difficult intubation.

Countries

Malaysia

Outcome results

None listed

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