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OpenTrials
Completed

NCT Number: NCT04276831

Comparison Between Laryngoscope McCoy With Macintosh

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

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Key information

Conditions

Surgery

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Indonesia University

Jakarta, DKI Jakarta, 10430, Indonesia

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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)

Treatment and study plan

Laryngoscope McCoy

Device

Subjects who fulfill inclusion criteria will be intubated using laryngoscope McCoy

Laryngoscope Macintosh

Device

Subjects who fulfill inclusion criteria will be intubated using laryngoscope Macintosh

Primary outcomes

  1. Measurement of systolic blood pressure

    Time frame: 3 minutes

    Measurement of systolic blood pressure by using automated sphygmomanometer and recorded in mmHg

  2. Measurement of diastolic blood pressure

    Time frame: 3 minutes

    Measurement of diastolic blood pressure by using automated sphygmomanometer and recorded in mmHg

  3. Measurement of mean arterial pressure

    Time frame: 3 minutes

    Measurement of mean arterial pressure by using automated sphygmomanometer and recorded in mmHg

  4. Measurement of heart rate

    Time frame: 3 minutes

    Measurement of heart rate and recorded beats per minute

Secondary outcomes

  1. Concentration of opioid administration for 24 hours after surgery

    Time frame: 24 hours

    Concentration of opioid administration in mcg

Sponsors and collaborators

Lead sponsor

Indonesia University

Other

Registry information

Official study title

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

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Feb 19, 2020
Registry last updated
Feb 19, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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