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Comparison of two different endotracheal tubes for intubation through Laryngeal Mask Airway BlockBuster® in children

A randomized controlled trial to compare blind endotracheal intubation with BlockBuster tube and silicone wire reinforced tube through Laryngeal Mask Airway BlockBuster® in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036444
Enrollment
90
Registered
2021-09-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Blind endotracheal intubation through Laryngeal Mask Airway BlockBuster® in children: To compare blind endotracheal intubation with BlockBuster tube and silicone wire reinforced tube t

Sponsors

Lady Hardinge Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Weight of 5 to 30 kg ASA Physical status I and II

Exclusion criteria

Exclusion criteria: 1. Anticipated difficult airway 2. Upper respiratory tract infection 3. Risk of aspiration

Design outcomes

Primary

MeasureTime frame
The proportion of patients with successful intubation in first attempt through BlockBuster LMA® in BlockBuster tube group and silicone wire reinforced tube groupTimepoint: within two minutes—

Secondary

MeasureTime frame
â?¢Proportion of patients requiring application of manoeuvres â?¢Proportion of patients requiring 2nd or 3rd attempt at intubation â?¢Mean (± SD) time in seconds taken for intubation â?¢Hemodynamic changes - Mean (± SD) HR, SBP, DBP, SpO2 â?¢Proportion of patients developing post extubation complications Timepoint: within two minutes, zero, two and four hours after extubation—

Countries

India

Contacts

Public ContactDr Ranju Singh

Lady Hardinge Medical College

ranjusingh1503@yahoo.com9811151285

Outcome results

None listed

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