Skip to content

To study and compare the two different devices-LMA BlockBuster and i-Gel used for airway patency during General Anaesthesia for surgery in Children

Evaluation and Comparison of insertion of LMA BlockBuster with i-Gel for airway management in children - NIL

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/064261
Enrollment
50
Registered
2024-03-18
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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: Blockbuster Laryngeal Mask Airway: Blockbuster Laryngeal Mask Airway of size appropriate for the weight of the patient will be used after induction during General Anaesthesia and will b

Sponsors

Pt. BD Sharma PGIMS, Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA category 1 or 2 with MPG I or II undergoing elective surgical procedures under general anaesthesia will be included in the study and appropriate size of the airway devices will be used.

Exclusion criteria

Exclusion criteria: Abnormal airway, refusal for informed written consent by the parent/ guardian, inadequate mouth opening (less than 2 finger breadth)

Design outcomes

Primary

MeasureTime frame
To study and compare the time of insertion of the devices usedTimepoint: Measured during induction of general anaesthesia

Secondary

MeasureTime frame
Blood stain, Laryngospasm, sore throat, cough, hoarseness of voiceTimepoint: Measured at extubation & at 1 hour, 3 hours & 6 hours post-operative period;Ease of insertionTimepoint: Assessed at baseline;Fiberoptic view scoringTimepoint: Assessed at baseline;Number of attemptsTimepoint: Assessed at baseline;Oropharyngeal leak pressureTimepoint: assessed at baseline

Countries

India

Contacts

Public ContactDr Komal Yadav

Pt. BD Sharma PGIMS, Rohtak

rao.komal96@gmail.com9899052990

Outcome results

None listed

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