Comparison Between Rigid Video Assisted Laryngoscopy vs Flexible Laryngoscopy in Anticipated Difficult Intubation

NCT ID: NCT04628611

Last Updated: 2020-11-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

106 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-01

Study Completion Date

2020-02-01

Brief Summary

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This is a randomized control study where adult patients had been divided randomly into two equal groups using video laryngoscope in group (V) and flexible intubating laryngoscope in group (F)

Detailed Description

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Routine pre-operative assessment including history taking, clinical examination, and laboratory tests. Patients were admitted to the operating room with a small 20G IV cannula after applying inclusion \& exclusion criteria and airway assessment by applying El Ganzuri multivariate risk index for difficult intubation which include assessment of the following : inter-incisor gap, Mallampati classification, head \&neck movement, buck teeth prognathism, thyromental distance, body weight and history of difficult intubation.

Operating room was prepared using :

Difficult airway cart that includes different size oral airways, endotracheal tubes, different sizes face masks \& laryngeal airway masks Suction apparatus to be ready for use Video laryngoscopy The flexible intubating laryngoscopy with the tube mounted over the fiberscope before the procedure.

Standard monitoring devices were applied including ECG, non invasive blood pressure. pulse oximetry and capnography after intubation Patients were then pre-oxygenated via face mask for three minutes and using 0.01 mic/kg atropine then general anesthesia is induced using fentanyl 1-2 mic/kg followed by propofol 2 mg/kg and esmeron 0.5 mg/kg.

The patient is mechanically ventilated using face mask until full relaxation is established after 3-5 minutes. The intubation is done using video laryngoscope in group (v) or using flexible intubating laryngoscopy in group (f) In the first group (v) The video laryngoscope was introduced with the patient appropriately positioned, the operator used the left hand to introduce the video laryngoscope into the midline of the Oropharynx and gently advances until the blade tip pass the posterior portion of the tongue. Using video visualization, the ETT was then advanced on a smooth curve through the glottis and intubation proceeds. Viewing the entire insertion step on the video screen allows the operator to quickly become facile with the motion of gently rotating or angling the tube using the right hand to redirect as necessary.

In the second group(f) patients positioned supine with the operator standing at the head of the bed. Simple chin lift and jaw thrust may improve the view through the flexible laryngoscopy and also help to prevent airway obstruction. The endotracheal tube should be lubricant to facilitate its subsequent advancement into the trachea. Once the endotracheal tube is in place, the scope is removed, and the patient is ventilated. Flexible intubating laryngoscopy is often performed with the operator looking through the eyepiece. However, connecting the flexible laryngoscopy to a monitor is often advantageous.

After collecting demographic data of the patient (age, sex, body mass index \& ASA) The following parameters will be measured :

Intubation time, Hemodynamic parameters, success rate and number of attempts \& incidence of complications.

Conditions

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Intubation

Keywords

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video laryngoscopy Flexible intubating bronchoscope Anticipated difficult intubation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

two equal groups; group (V) using video laryngoscope(53) and group (F) using flexible intubating laryngoscopy(53).
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
the participant does not know which group the patient belongs to as every patient was consented for both devices which were ready in the operating theatre

Study Groups

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Video laryngoscopy Group (V) using Storz c-mac laryngoscope

video laryngoscope without a channel used for endotracheal intubation, the device used to obtain a view of the larynx, and the endotracheal tube is passed through the vocal cords independent of the device. The device is connected to the monitor via connecting cable

Group Type ACTIVE_COMPARATOR

Video laryngoscopy

Intervention Type DEVICE

Endotracheal intubation using video laryngoscopy

The flexible intubating laryngoscopy Group (F) using Storz flexible intubation video endoscope set

The flexible intubating scope is used to locate the vocal cords and acts as a stylet for the endotracheal tube once the scope is placed into the trachea.This device consists of a flexible insertion cord that contains a small camera at the tip, used to transmit images to camera head. The cord includes a channel for a light source, a working channel for suction or administration of oxygen or local anesthetic, and a cable that allows the operator to flex the tip of the scope. The cord attaches to a handle with a light source,camera head control lever for flexion/extension of the tip, and a working channel port. The device is connected to the monitor via connecting table

Group Type ACTIVE_COMPARATOR

Flexible intubating laryngoscopy

Intervention Type DEVICE

Endotracheal intubation using flexible intubating laryngoscope

Interventions

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Video laryngoscopy

Endotracheal intubation using video laryngoscopy

Intervention Type DEVICE

Flexible intubating laryngoscopy

Endotracheal intubation using flexible intubating laryngoscope

Intervention Type DEVICE

Other Intervention Names

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Storz c-mac laryngoscopy Storz flexible intubation video endoscope set

Eligibility Criteria

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Inclusion Criteria

1. El-Ganzouri score: 2, 3, 4 (Table 1)
2. American Society of Anesthesiology (ASA) I, II, III
3. Elective surgeries

Exclusion Criteria

1. Refusal of participation
2. Patients who need a surgical airway (e.g. patients with highly obstructing laryngeal lesions such as cancer tongue, larynx\& maxilla).
3. Patients with laryngeal trauma, especially in those with suspected cricotracheal separation.
4. Patients with craniofacial trauma.
Minimum Eligible Age

20 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute, Egypt

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Essam AH Mahran, MD

Role: STUDY_DIRECTOR

Assistant Professor of Anesthesia, ICU, and Pain Management, NCI, Cairo

Other Identifiers

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IORG000381

Identifier Type: -

Identifier Source: org_study_id