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A study to compare blind tracheal intubation with two different types of endotracheal tubes through a supraglottic device in children

A randomized controlled trial to compare blind endotracheal intubation with cuffed PVC tube and silicone wire reinforced tube through second generation laryngeal mask airway in children - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074069
Enrollment
240
Registered
2024-09-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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: Blind tracheal intubation via second generation LMA using PVC tube or wire reinforced tube in pediatric patients undergoing surgery under general anesthesia : Group 1- Blind tracheal i

Sponsors

Lady Hardinge Medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Weight of 5 to 50 Kg ASA physical status 1 and 2

Exclusion criteria

Exclusion criteria: Anticipated difficult airway upper respiratory tract infection Risk of aspiration

Design outcomes

Primary

MeasureTime frame
The proportion of patients with successful intubation in first attempt through second generation laryngeal mask airway in group 1 and group 2Timepoint: Baseline - that is taken as the time at which general anesthesia is induced and endotracheal intubation is accomplished

Secondary

MeasureTime frame
1.Number of patients requiring application of maneuvers 2. Proportion of patients requiring 2nd attempt at intubation 3.Mean time taken in seconds for intubation 4.Proportion of patients developing post operative sore throat Timepoint: Two and four hours after extubation

Countries

India

Contacts

Public ContactDr Monika Yadav

Lady Hardinge Medical College

yadavmonika1234@gmail.com9560918485

Outcome results

None listed

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