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Laryngoscopes comparison

A PROSPECTIVE RANDOMIZED COMPARATIVE STUDY OF MACINTOSH LARYNGOSCOPE WITH USB VIDEO LARYNGOSCOPE IN EASE OF INTUBATION AND HAEMODYNAMIC DERANGEMENTS - Airway

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/07/014986
Enrollment
60
Registered
2018-07-20
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- ASA Grade I and II

Interventions

Intervention1: USB Video Laryngoscope: To Compare the laryngoscopy and intubation time Control Intervention1: Macintosh laryngoscope: To compare laryngoscopy and intubation time

Sponsors

Department Of Anaesthesiology
Lead Sponsor
Syed Hussain Amir
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: ASA Grade I & II patients. Age between 25-60 years Weight between 45-70 kg Patients of either sex(male/female) Patients planned for elective surgery

Exclusion criteria

Exclusion criteria: Previous history of multiple/ failed intubation. Predicted difficult laryngoscopy except for all class of MP Grades Any pathology of the oral cavity that may obstruct the insertion of device Mouth opening less than 2.5cm. Potentially full stomach patients (trauma, morbid obesity, pregnancy, history of gastric regurgitation and heart burn) and at risk of esophageal reflux (hiatus hernia).

Design outcomes

Primary

MeasureTime frame
To compare the laryngoscopy & intubation time using the two intubating devices. To compare the number of attempts required for successful intubation To grade the ease of tracheal intubation using these devices Timepoint: two years

Secondary

MeasureTime frame
To compare the glottic view using Cormack and Lehane Grading. To compare the number of adjustment maneuvers required for successful intubation. To compare changes in heart rate and mean arterial blood pressure during laryngoscopy and intubation using the two devices. To look for any trauma during laryngoscopy and intubation. To record the incidence of postoperative sore throat within 24 hrs. Timepoint: two years

Countries

India

Contacts

Public ContactQazi Ehsan Ali

Jawaharlal Nehru Medical College

qaziehsanali@gmail.com7417701769

Outcome results

None listed

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