Skip to content

Comparison of success rates of two airway gadgets as conduits for blind endotracheal intubation in patients with anticipated difficult airway.

Comparison of success rates of BlockbusterTM LMA with Air – Q ILATM as conduits for blind endotracheal intubation in patients with anticipated difficult airway: A prospective randomised trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058862
Enrollment
30
Registered
2023-10-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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: O- Medical and Surgical Health Condition 3: O- Medical and Surgical Health Condition 4: R098- Other specified symptoms and signsinvolving the circulatory and respiratory systems

Interventions

Intervention1: Group B – Blockbuster LMA: The appropriately sized Blockbuster LMA using weight-based formula lubricated with water-based jelly will be inserted by an experienced anesthesiologist by st

Sponsors

AIIMS Mangalagiri
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients belonging to the age group 18 to 65 years. 2. ASA Physical Status of I – III. 3. Mallampatti Grade of III and IV. 4. Wilson’s score of = 6. 5. Scheduled for surgery under general anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients belonging to the age group less than 18 and above 65 years. 2. ASA Physical Status of IV and above. 3. Mallampatti Grade of I and II. 4. Wilson’s score of = 5. 5. Predictors of difficult LMA insertion. 6. Patients who are at risk of aspiration. 7. Surgeries of the head and neck region, major abdominal surgeries and surgeries in the prone position.

Design outcomes

Primary

MeasureTime frame
The primary objective is to compare the success rate of blind tracheal intubation at the first attempt between LMA Blockbuster and Air – Q ILA in patients with an anticipated difficult airway.Timepoint: At baseline, at the time of intubation and extubation, and at 2 hours after surgery.

Secondary

MeasureTime frame
Ease of insertion, the time and number of attempts taken to insert the SGAD, 1st attempt success rate, the grade of laryngeal view attained using a fibreoptic bronchoscope, time for successful intubation.Timepoint: At baseline and at the time of intubation;To assess the incidence of other airway related complications like sore throat, trauma, laryngospasm and bronchospasm in the perioperative period.Timepoint: At the time of extubation and at 2 hours after surgery.

Countries

India

Contacts

Public ContactDr ghansham Biyani

All India Institute of Medical Sciences, Mangalagiri

drghanshambiyani@aiimsmangalagiri.edu.in8764439671

Outcome results

None listed

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