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A clinical trial to evaluate Glidescope Video Laryngoscope.

A comparative evaluation of GlideScope and Macintosh laryngoscope for endotracheal intubation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/08/003889
Enrollment
200
Registered
2013-08-08
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- ease of endotracheal intubation

Interventions

Intervention1: GlideScope: A comparative evaluation of GlideScope and Macintosh laryngoscope for endotracheal intubation Control Intervention1: Macintosh laryngoscope: A comparative evaluation of Glid

Sponsors

Govt Medical College and Hospital Sector Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age group of 18 to 60 years 2.ASA(American Society of Anesthesiologists) physical status I /II 3.Patients undergoing elective surgery requiring general anaesthesia with endotracheal intubation.

Exclusion criteria

Exclusion criteria: 1.Morbid obesity BMI > 35KG/m2 2.Known airway pathology (oropharynx, larynx ) 3.Patients at increased risk of aspiration like gastroesophageal reflux, peptic ulcer 4.Previous upper gastrointestinal surgery 5.Pregnancy 6.Coagulopathy or history of anticoagulant use 7.Cardiorespiratory or cerebrovascular disease 8.Cervical spine injury

Design outcomes

Primary

MeasureTime frame
Ease of intubation will be assessed depending on 1.Time taken for intubation (TTI) 2.Number of attempts for endotracheal intubation. 3.Glottic view (Cormack &Lehane and POGO). 4.Need for other maneuvers like change of blade, patient position or applying external laryngeal pressure. Timepoint: All primary outcomes will be measured from the time of introduction of device in mouth to the confirmation of endotracheal tube placement by a square wave capnogram on the monitor.—

Secondary

MeasureTime frame
1.Heart Rate (HR), Systolic Blood Pressure (SBP), Diastolic Blood Pressure (DBP), Oxygen Saturation (SpO2), Electrocardiogram (ECG) and End tidal carbon (EtCO2 ) be monitored. 2.Any other intra or post operative findings and adverse events. Timepoint: 1.Hemodynamic parameters (HR, SBP, DBP, SpO2, ECG, EtCO2) will be recorded at 1 minute interval during intubation and at 5 minute interval for 15minutes after intubation. 2. Intra or post operative findings and adverse events will be documented during and after endotracheal intubation and post extubation.—

Countries

India

Contacts

Public ContactProf Satinder Gombar

Department of Anaesthesia and Intensive care, GMCH, Chandigarh

itallionstallion17@gmail.com9888122668

Outcome results

None listed

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