Comparison Between Laryngoscope McCoy With Macintosh

Comparison of Cardiovascular Response and Ease of Intubation Using Laryngoscope McCoy With Macintosh in Malay Race in Indonesia

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04276831

Enrollment

Registered

2020-02-19

Start date

2018-12-01

Completion date

2019-03-04

Last updated

2020-02-19

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

Conditions

Surgery

Keywords

Intubation, Cardiovascular response, Laryngoscope

Brief summary

This study aimed to compare cardiovascular response and ease of intubation using laryngoscope McCoy with Macintosh

Detailed description

Eighty-two subjects were given informed consent before enrolling the study and randomized into two groups: McCoy and Macintosh. Non-invasive blood pressure

Interventions

DEVICELaryngoscope McCoy

Subjects who fulfill inclusion criteria will be intubated using laryngoscope McCoy

DEVICELaryngoscope Macintosh

Subjects who fulfill inclusion criteria will be intubated using laryngoscope Macintosh

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

OTHER

Masking

SINGLE (Investigator)

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Yes

Inclusion criteria

: * adults (18 - 65 years old) * body mass index 18,5 - 30 kg/m2 * physical status with ASA 1 -2 * patients who agreed to participate in this study and sign informed consent.

Exclusion criteria

* pregnancy * history of infarct miocard * right or left heart failure * P-R interval 0,24 seconds * heart block degree 2 or 3 * using pace maker * history of cerebrovascular disease * tachycardia or bradycardia * on medication (antiarrhythmic drugs, beta blocker, heart stimulant) * suspect difficult airways * including ventilation (assesment with MOANS) or intubation (assesment with LEMONS) * patients with increase of intracranial pressure (e.g.head injury)

Design outcomes

Primary

Measure	Time frame	Description
Measurement of systolic blood pressure	3 minutes	Measurement of systolic blood pressure by using automated sphygmomanometer and recorded in mmHg
Measurement of diastolic blood pressure	3 minutes	Measurement of diastolic blood pressure by using automated sphygmomanometer and recorded in mmHg
Measurement of mean arterial pressure	3 minutes	Measurement of mean arterial pressure by using automated sphygmomanometer and recorded in mmHg
Measurement of heart rate	3 minutes	Measurement of heart rate and recorded beats per minute

Secondary

Measure	Time frame	Description
Concentration of opioid administration for 24 hours after surgery	24 hours	Concentration of opioid administration in mcg

Countries

Indonesia

Outcome results

None listed

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