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Evaluation of two different methods of video-laryngoscopy

Comparison of face-to-face tracheal intubation and conventional head-end tracheal intubation using video-laryngoscope in adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/12/016611
Enrollment
50
Registered
2018-12-11
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: H60-H95- Diseases of the ear and mastoid process Health Condition 2: M00-M99- Diseases of the musculoskeletal system and connective tissue Health Condition 3: K80-K87- Disorders of gallbladder, biliary tract and pancreas Health Condition 4: C50-C50- Malignant neoplasms of breast Health Condition 5: K55-K64- Other diseases of intestines

Interventions

Intervention1: Endotracheal intubation using video-laryngoscope: Endotracheal intubation will be done in adult patients of either sex posted for elective surgical procedures requiring general anaesthe

Sponsors

University College of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I-II Modified Mallampati Grade I and II Mouth opening >3 finger breadths Thyromental distance >6 cm BMI

Exclusion criteria

Exclusion criteria: Patients who do not give consent to participate in the study. Anticipated difficult bag mask ventilation and difficult intubation. Any airway tumor or prior neck or thyroid surgery. History of recent upper respiratory tract infection within past 15 days, cervical spine disorders, coagulation disorders. Patients having features of raised intracranial pressure Full stomach patients. Patients with cardiovascular, cerebral, renal, hepatic, bronchospastic and endocrine disease or psychiatric disorder.

Design outcomes

Primary

MeasureTime frame
Intubation timeTimepoint: Once, time taken from the device entering the oral cavity until observation of the tracheal tube entering through the vocal cords on the video-monitor.

Secondary

MeasureTime frame
Device Insertion timeTimepoint: once, time taken from the device entering the oral cavity until clear visualization of the glottis on the video-monitor.;Failed intubationTimepoint: once, at the end of intubation;Glottic viewTimepoint: once, at the end of intubation;Hemodynamic parameters; heart rate, systolic and diastolic blood pressure, mean arterial pressure and SpO2Timepoint: 1 min, 3 min, 5 min, 10 min and 15 min after intubation;Number of intubation attemptsTimepoint: once, at the end of intubation

Countries

India

Contacts

Public ContactDr Swati Bharti

University College of Medical Sciences, Delhi University

sujatac462@gmail.com9999051546

Outcome results

None listed

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