Skip to content

Comparison of two airway devices for endotracheal intubation using fibrescope.

Comparison of Blockbuster laryngeal mask with Air Q intubating laryngeal airway for fibreoptic endotracheal intubation. - NILL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054556
Enrollment
90
Registered
2023-06-30
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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: Fibreoptic intubation will be done with Blockbuster laryngeal mask using Blockbuster tube.: Patients will be intubated through Blockbuster laryngeal mask using Blockbuster tube under fi

Sponsors

Department of Anaesthesiology and Critical Care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients belonging to American Society of Anesthesiologists (ASA) physical status I-II having modified mallampati classification (MMT) I-II scheduled for elective surgery under general anaesthesia requiring endotracheal intubation.

Exclusion criteria

Exclusion criteria: Patients with pharyngeal pathology, aspiration risk ( Pregnancy, Hiatal hernia), low pulmonary compliance, cervical spine injury, poor dentition/loose teeth ,temporo-mandibular joint ankylosis ,restricted mouth opening =30 kg/m2 and who refuse to participate will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
First attempt success rate of fiberoptic guided tracheal intubation through designated supraglottic device using Blockbuster tube.Timepoint: At the time of appearance of square wave capnography after fibreoptic guided intubation.

Secondary

MeasureTime frame
Haemodynamic parameters Systolic blood pressure, Diastolic blood pressure, Mean arterial pressure & SpO2)Timepoint: 1- Baseline 2- 1 min after induction 3- 1 min after insertion of designated supraglottic device. 4- 1 min after insertion of endotracheal tube 5- 1 min after removal of study device.;Number of attempts for designated supraglottic device placement.Timepoint: At the time of confirmation of successful supraglottic device placement.;Number of attempts for insertion of fibreoptic guided endotracheal tube through designated supraglottic device.Timepoint: At the time of confirmation of successful endotracheal tube placement.

Countries

India

Contacts

Public ContactShikha

Pt B D Sharma PGIMS, Rohtak

dr.jatinlal@gmail.com9728265511

Outcome results

None listed

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