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Comparison of Airway management using AIROD and Gum elastic Bougie.

A Comparative evaluation of AIROD vs Gum elastic Bougie as an intubation adjunct in simulated difficult airway. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068659
Enrollment
70
Registered
2024-06-11
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 Health Condition 2: X- New Technology

Interventions

Intervention1: AIROD: Standardized anaesthesia protocol will be followed. The cervical collar will be placed around the neck to create a simulated difficult airway. Pre-oxygenation for 3 minutes will

Sponsors

Pt BD Sharma University of Health Sciences PGIMS Rohtak Haryana
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Seventy patients of either sex aged 18-60 years belonging to American Society of Anaesthesiologists (ASA) physical status I or II scheduled for elective surgery under general anaesthesia requiring endotracheal intubation will be included in the study.

Exclusion criteria

Exclusion criteria: Patients having respiratory or pharyngeal pathology,restricted mouth opening,Body mass index more than 30,pregnancy,full stomach,anticipated difficult airway and any patient who refuses to participate in the study will be excluded from the study

Design outcomes

Primary

MeasureTime frame
To compare the first pass success rate of intubation through AIROD and gum elastic bougie.Timepoint: Baseline MAP, HR and SPO2 will be recorded. Thereafter values will be recorded after induction, and at 1st, 3rd and 5th minute after successful intubation.

Secondary

MeasureTime frame
Number of attempts taken to insert the introducer,Ease of passing the introducer ,Total time taken for successful intubation,Ease of intubation ,Optimisation manoeuvres required for intubation ,Haemodynamic variation ,Complications secondary to device placement. Timepoint: Baseline MAP, HR and SPO2 will be recorded. Thereafter values will be recorded after induction, and at 1st, 3rd and 5th minute after successful intubation.

Countries

India

Contacts

Public ContactDr Vikash

Pt. BD Sharma PGIMS Rohtak

panwarvikash93@gmail.com9467002626

Outcome results

None listed

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