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A STUDY COMPARING CONVENTIONAL MACINTOSH LARYNGOSCOPE WITH VIDEOLARYNGOSCOPE FOR NASOTRACHEAL INTUBATION

A RANDOMISED CONTROLLED STUDY COMPARING CONVENTIONAL MACINTOSH LARYNGOSCOPE WITH VIDEOLARYNGOSCOPE FOR NASOTRACHEAL INTUBATION

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057172
Enrollment
74
Registered
2023-09-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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: Nasotracheal intubation: All patients will be intubated with their heads in sniffing position. The appropriate flexometallic endotracheal tube of the size 7/7.5/8.0/8.5 as per discretio

Sponsors

Bharati Hospital and Research Centre
Lead Sponsor
Bharati Hospital and Research Centre
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: INCLUSION CRITERIA: 1.Patients who are undergoing elective surgery requiring nasotracheal intubation under GA 2.MP-I and MP-II patients 3.ASA-I and ASA-II patients. 4.Age group of 18-60 years.

Exclusion criteria

Exclusion criteria: EXCLUSION CRITERIA: 1.Refusal of consent. 2.Anticipated difficult airway 3.Emergency surgery 4.Those at increased risk of aspiration

Design outcomes

Primary

MeasureTime frame
Outcome measured are: 1. Time required for intubation, which is considered as the time from insertion of laryngoscope to appearance 1st square wave form of capnograph will be defined as time to successful intubation. 2. Heart Rate 3. Blood Pressure 4. Need for External maneuvers 5. Attempts required for intubation.Timepoint: Time points are: T0- first observation when patient is bought to operation theatre. T induction- observation at the time General anesthesia induction T intubation- observation at the time of intubation T1,T2,T4,T8,T10 are observation at 1,2,4,8,10 minutes respectively after intubation.

Secondary

MeasureTime frame
Need for external laryngeal manipulation and use of Magill’s forceps will be recorded.Timepoint: Haemodynamic parameters (HR,MAP) will be recorded from 1,2, 5, 8& 10 mins from intubation.

Countries

India

Contacts

Public ContactDrKalyani Patil

Bharati Hospital and Research Centre

kalyanish19@gmail.com9673400066

Outcome results

None listed

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