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A study to see how easy it is to insert a breathing tube using the Blockbuster airway device

A Prospective Study on the Ease of Endotracheal Intubation Using the Blockbuster Laryngeal Mask Airway (LMA) - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/106048
Enrollment
60
Registered
2026-03-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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: Nil: Nil Intervention2: Nil: Nil

Sponsors

Vinayaka Missions Kirubanandha Variyar Medical College and Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA (American Society of Anesthesiologists) physical status I or II, Patients undergoing elective surgical procedures under general anesthesia, Mallampati score I or II

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
To determine the first attempt success rate of endotracheal intubation through the Blockbuster LMA and To evaluate the perfect positioning of the LMA time taken for LMA insertion and for Endotracheal intubationTimepoint: Time taken for LMA insertion (0 minutes) , Perfect positioning of LMA Immediately after insertion (0 minutes) First-attempt success and time taken for endotracheal intubation Immediately after successful ETT placement (30 seconds )

Secondary

MeasureTime frame
To compare postoperative complications, Sore Throat, Hoarseness of Voice, Dysphagia, Coughing or Laryngospasm, Gastric Distension within the first 24 hoursTimepoint: Post operative complications are assessed immediately after removing device 0 hour, 2 hours, 6 hours , 12 hours 24 hours post operatively

Countries

India

Contacts

Public ContactDr Brindha

Vinayaka Missions Kirupananda Variyar Medical College and Hospital

venkatagopijalemedico@gmail.com9443247021

Outcome results

None listed

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