"Comparison of two nonchannelled videolaryngoscopes with standard direct laryngoscope for endotracheal intubation in adult patients undergoing elective surgery."

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/03/012835

Enrollment

180

Registered

2018-03-26

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- Adult patients (18-65)years of either gender with ASA grade I and II

Interventions

Intervention1: Videolaryngoscope(VL): Patients in this group will be given general anaesthesia(induction with inj Fentanyl 2mcg/kg iv, inj Propofol 2mg/kg iv, and inj vecuronium 0.1kg/mg iv.) After in

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I and II, having BMI <=30kg/m2 and standard airway parameters within normal range, scheduled for elective surgery under general anaesthesia requiring endotracheal intubation.

Exclusion criteria

Exclusion criteria: 1. Patients who have anticipated difficult airway and modified Mallampati class III or IV 2. Haemodynamic instability, hypertion, morbid obesity, cardiac, renal, hepatic, endocrine, pulmonary dysfunction, upper respiratory tract infection. 3. Cervical spine instability. 4. Pregnancy

Design outcomes

Primary

Measure	Time frame
To comparatively evaluate the first attempt success rate for endotracheal intubationTimepoint: At the time of intubation.	—

Secondary

Measure	Time frame
To comparatively eveluate the modified Cormac-Lehane view, time and ease of laryngoscopy and intubationTimepoint: At the time of intubation.	—

Countries

India

Contacts

Public ContactDr Prachi Abhyankar

Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi

nikkisabharwal162@gmail.com9810774396

Outcome results

None listed

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