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To compare efficacy of BlockBuster Laryngeal Mask Airway with that of AmbuAuraGain for ventilation in paediatric patients undergoing elective surgery under general anaesthesia

Comparison of efficacy of two anatomically preformed supraglottic devices for ventilation in paediatric patients undergoing elective surgery under general anaesthesia - NIL

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068284
Enrollment
70
Registered
2024-06-04
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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: AmbuAuraGain: Oropharyngeal seal pressure will be noted within 5 minutes after device insertion and the next reading will be taken after 30 minutes of device insertion. Control Interven

Sponsors

Vardaman Mahavir Medical
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologist Physical Status I and II and undergoing elective surgical procedures under general anaesthesia with controlled ventilation

Exclusion criteria

Exclusion criteria: 1. Patients with anticipated difficult airway 2. Anticipated surgery time greater than 4 years 3. High risk of aspiration

Design outcomes

Primary

MeasureTime frame
To compare oropharyngeal seal pressure of BlockBuster Laryngeal Mask airway with that of AmbuAuraGain in paediatric patients undergoing elective surgery under general anaesthesiaTimepoint: Oropharyngeal seal pressure will be noted within 5 minutes after device insertion and the next reading will be taken after 30 minutes of device insertion.

Secondary

MeasureTime frame
To compare following insertion characteristics of BlockBuster Laryngeal mask airway with that of Ambu AuraGainTimepoint: Number of attempts taken for successful insertion of the device. Time taken for achieving effective ventilation . Ease of insertion of device & gastric catheter. Anatomical alignment of the device to glottis opening by Brimacombe score. These parameters will be measured within a duration of half an hour.

Countries

India

Contacts

Public ContactDr Nidhi Agrawal

Vardaman Mahavir Medical College And Safdarjung Hospital, New Delhi

nidhi.agrawal1970@gmail.com9811030408

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jul 3, 2026