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Comparison of hemodynamic changes between tracheal intubation with Mackintash Laryngoscop and Glidescope

Comparison of hemodynamic changes between tracheal intubation with Mackintash Laryngoscop and Glidescope

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201111264969N4
Enrollment
104
Registered
2011-12-20
Start date
2011-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

blood pressure and heart rate changes after tracheal intubation.

Interventions

Intervention 1: laryngoscopy with mackintash laryngoscop. Intervention 2: laryngoscopy with glidescope (video laryngoscop).
laryngoscopy with mackintash laryngoscop
laryngoscopy with glidescope (video laryngoscop)

Sponsors

Tehran University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- ASA physical status 1 or 2 2- Mallampati classification 1 or 2 3- Aged between 18 and 60 4- Baseline BP less than 140/90 5- Patients without history of difficult intubation or laryngoscopy 6- Patients without history of cervical spine disease, GERD, and pulmonary disease 7- Patients without difficult laryngoscopy or intubation. 8- Body mass index = 30 Exclusion criteria: 1- Patients failed to be ventilated by face mask following induction of anesthesia 2- Decrease more than 25% in heart rate (HR) and blood pressure (BP) after induction of anesthesia 3- Decrease in O2 saturation to = 94% during ventilation or intubation 4- Cormack and Lehane score more than 2 at laryngoscopy 5- Failed intubation attempt which defined as patients requiring more than one attempt to achieve successful intubation, intubations that require more than 30s to be performed and also need for another person to complete the procedure. 6- Patients taking antihypertensive or other medications affecting on HR and BP such as ß-blockers, and calcium channel blockers

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure. Timepoint: every 3 minutes. Method of measurement: automatic.;Diastolic blood pressure. Timepoint: every 3 minutes. Method of measurement: automatic.;Heart rate. Timepoint: every 3 minutes. Method of measurement: puls oxymeter.

Secondary

MeasureTime frame
Sorethroat. Timepoint: after surgery (recovery room). Method of measurement: asking the patient and observation.;Horseness. Timepoint: after surgery (recovery room). Method of measurement: asking the patient and observation.;Intubation time. Timepoint: during intubation. Method of measurement: chronometer.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026