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Comparison Between Laryngoscope McCoy With Macintosh

U

University of Indonesia (UI)

Status

Completed

Conditions

Surgery

Treatments

Device: Laryngoscope McCoy
Device: Laryngoscope Macintosh

Study type

Interventional

Funder types

Other

Identifiers

NCT04276831
IndonesiaUAnes046

Details and patient eligibility

About

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

Full description

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

Enrollment

82 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

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)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

82 participants in 2 patient groups

Laryngoscope McCoy
Active Comparator group
Description:
Patients will be intubated using laryngoscope McCoy
Treatment:
Device: Laryngoscope McCoy
Laryngoscope Macintosh
Active Comparator group
Description:
Patients will be intubated using laryngoscope Macintosh
Treatment:
Device: Laryngoscope Macintosh

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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