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Blockbuster laryngeal mask airway versus Fastrach laryngeal mask airway for blind tracheal intubation.

A study of Blockbuster laryngeal mask airway versus Fastrach/Intubating laryngeal mask airway as a conduit for blind orotracheal intubation : A prospective randomised controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/12/029655
Enrollment
100
Registered
2020-12-09
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: H60-H95- Diseases of the ear and mastoid process

Interventions

Intervention1: Blockbuster Laryngeal mask airway: Blind orotracheal intubation through Blockbuster Laryngeal mask airway in patients posted for elective surgery requiring endotracheal intubation (5 ca

Sponsors

SSG HOSPITAL VADODARA
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)weight 30-70 kgs 2)american society of anaesthesiology grade 1 or 2 3)posted for elective surgeries requiring general anaesthesia with oral endotracheal intubation

Exclusion criteria

Exclusion criteria: 1)Patients with predicted difficult airway (mouth opening of less than 2.5cm, mallampati class 3 or 4, cervical spine deformitied, neck and jaw deformities) 2)Patients with BMI more than 25 kg per m2 3) Patients with urti, oro-pharyngeal pathology, history of gastro-oesophageal reflux disease, allergy to any drugs used in the study 4)Pregnant females 5)Patients not willing for participation

Design outcomes

Primary

MeasureTime frame
1)the success rate of blind oro-tracheal intubation through Fastrach LMA and Blockbuster LMA 2)Number of attempts of LMA insertion 3)Time taken for LMA insertion 4)Ease of insertion of LMA 5)Number of attempts of tracheal intubation 6)Time taken for tracheal intubation through LMA 7)Ease of tracheal intubation through LMA Timepoint: during induction of anaesthesia

Secondary

MeasureTime frame
1)To compare the hemodynamic parameters. 2) To observe for complications related to the devices if any. Timepoint: during induction of anaesthesia, intraoperatively and postoperatively

Countries

India

Contacts

Public ContactDr Komal Modi

S.S.G Hospital Vadodara

komaltmodi@gmail.com9712998276

Outcome results

None listed

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