Comparison of 2 methods of putting the patients to sleep with new technique using camera enabled viewing.

Comparison of Fiberoptic intubation with video assisted fiberoptic intubation in predicted difficult airway: A randomised controlled trial - nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/068190

Enrollment

Registered

2024-05-31

Start date

Unknown

Completion date

Unknown

Last updated

2024-06-24

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: VAFI Group: Endotracheal intubation will be performed by Fiberoptic bronchoscope and videolaryngoscope after 4 minutes of induction. Control Intervention1: FOB Group: Endotracheal intub

Eligibility

Inclusion criteria

Inclusion criteria: ASA status I and II in the age range of 18-65 years patients of either gender undergoing elective surgery requiring endotracheal intubation having at least 1 predictor of difficult intubation

Exclusion criteria

Exclusion criteria: Patient’s Refusal mouth opening ( less than 22mm) Bleeding Disorders ASA Physical status 4 or higher Patients planned for Awake FOB will be excluded.

Design outcomes

Primary

Measure	Time frame
Time to intubationTimepoint: immediately after intubation	—

Secondary

Measure	Time frame
Glottic viewTimepoint: 30 seconds after laryngoscopy;Hemodynamic changesTimepoint: o minute, 1 minute, 3 minute, 5 minute, 10 minute, 15 minute after intubation;hypoxemiaTimepoint: 1 minute after intubation;Success rateTimepoint: 1 minute after intubation	—

Countries

India

Contacts

Public ContactDivya

Postgraduate institute of medical education and research

Jaindivya77@rediffmail.com09855900171

Outcome results

None listed

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