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A comparison of modern video technique and traditional method for putting a breathing tube in emergency patients

Comparison of videolaryngoscopy versus conventional laryngoscopy for endotracheal intubation in emergency department - a prospective interventional study - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/09/094006
Enrollment
50
Registered
2025-09-01
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Endotracheal Intubation: Patients requiring intubation and mechanical ventilation Intervention2: Videolaryngoscopy-assisted endotracheal intubation: One time oral endotracheal intubatio
performed by the principal investigator after prior training. Standard ED RSI meds and pre-oxygenation as per protocol (not part of the intervention). Bougie or stylet may be used if needed. Tube posi

Sponsors

Dr Ritu Khandelwal
Lead Sponsor
Datta Meghe Institute of Higher Education Research
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients in need of emergency endotracheal intubation

Exclusion criteria

Exclusion criteria: Pregnant females. Morbidly obese patients. Refusal to participate in study by relatives.

Design outcomes

Primary

MeasureTime frame
Attempt is defined as any insertion of either a direct laryngoscope or videolaryngoscope into the patient?s mouth. Number of attempts required for successful intubation will be recorded. First pass success rate, defined when the blade was applied for the first time and the endotracheal tube was passed through the vocal cords in the same attempt. Incidence of first pass success rate will be recorded. Time to intubation, defined as the time from when the laryngoscope is first placed into the patient?s mouth until confirmation of ETT on capnography will be recorded Timepoint: 18 Months

Secondary

MeasureTime frame
Intubation related adverse events, including major and minor adverse events within 30 mins of intubation will be recorded.Timepoint: 18 Months

Countries

India

Contacts

Public ContactDr Ritu Khandelwal

Datta Meghe Institute of Higher Education & Research

charutagadkari@gmail.com9823017279

Outcome results

None listed

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