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McGrath vs. C-MAC Video Laryngoscopy Comparison in Endotracheal Tube Insertion

NCT ID: NCT04936516

Last Updated: 2021-10-19

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

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-08-01

Study Completion Date

2021-10-14

Brief Summary

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Tracheal intubation is commonly performed using a standard Macintosh blade, but recently there has been advanced technology using video laryngoscopy (VL).In this modern era, there are various types of available VL to make it easier for anesthesiologists to perform intubation, especially in patients with difficult airway anatomy.

Various studies showed different results regarding the effectiveness of both C-MAC® and McGrath®, by assessing the comparison of the effectiveness, valuable information will be obtained for further consideration by experts in choosing the best tools in the future.

Detailed Description

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Conditions

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Intubation; Difficult or Failed

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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McGrath Video Laryngoscope

Group Type ACTIVE_COMPARATOR

Endotracheal intubation

Intervention Type DEVICE

Endotracheal intubation using either McGrath or C-MAC video laryngoscopy

C-MAC Video Laryngoscope

Group Type ACTIVE_COMPARATOR

Endotracheal intubation

Intervention Type DEVICE

Endotracheal intubation using either McGrath or C-MAC video laryngoscopy

Interventions

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Endotracheal intubation

Endotracheal intubation using either McGrath or C-MAC video laryngoscopy

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Elective surgery patients without neck and face trauma
2. Undergo surgery requiring general anesthesia with endotracheal intubation
3. Patients with physical status ASA I-III
4. Patients aged 18-65 years
5. Nutritional status (BMI \< 35 Kg/m2)

Exclusion Criteria

1. Patients refusal to be included in the study
2. Patients with cervical spine instability
3. Anatomical and structural abnormalities of the maxillary teeth
4. Thyromental distance \<6 cm and inter-incisor distance \<3.5 cm
5. History of difficult intubation
6. LEMON criteria ≥ 3
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Udayana University

OTHER

Sponsor Role lead

Responsible Party

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Christopher Ryalino, MD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Tjokorda GA Senapathi, Dr

Role: STUDY_CHAIR

Udayana University

Jhoni P Pasaribu

Role: STUDY_DIRECTOR

Udayana University

Christopher Ryalino

Role: PRINCIPAL_INVESTIGATOR

Udayana University

Locations

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Sanglah General Hospital

Denpasar, Bali, Indonesia

Site Status

Countries

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Indonesia

Other Identifiers

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UNUD-CTR-FK110621-001

Identifier Type: -

Identifier Source: org_study_id