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comparision of BlockBuster LMA intubating LMA

A study to compare the ease of intubation using intubating LMA and LMA BlockBuster

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/12/038727
Enrollment
54
Registered
2021-12-17
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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 LMA: Peripheral intravenous line will be secured with appropriate sized cannula. Pre-oxygenation for 3 minutes will be done with 100% oxygen. Induction of anaesthesia will b

Sponsors

Department of Anaesthesiology and critical care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Sixty patients of either sex aged 18-60 years belonging to American Society of Anaesthesiologists (ASA) physical status 1 or 2 scheduled for elective surgery under general anaesthesia requiring endotracheal intubation will be included in the study.

Exclusion criteria

Exclusion criteria: atients having respiratory or pharyngeal pathology, mouth opening 30kgm -2 , pregnancy, full stomach, anticipated difficult airway will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
success rate of intubation Timepoint: ease of intubation will be assessed for both intubating and BlockBuster LMA. Data will be compiled and appropriate statistical test will be used to analyse the results.

Secondary

MeasureTime frame
Success of placement of LMA Time taken for intubation Number of attempts ï?· Haemodynamic variation ï?· Pharyngo-laryngo morbidityTimepoint: Following will be assessed for both intubating and BlockBuster LMA. Data will be compiled and appropriate statistical test will be used to analyse the results.

Countries

India

Contacts

Public ContactDr Vishvas Verma

PGIMS Rohtak

kiranpreet72@rediffmail.com9467807441

Outcome results

None listed

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