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Comparison between two devices for securing airway access in patients undergoing general anaesthesia

Comparison of Blind Oro-Tracheal Intubation through LMA Blockbuster and LMA Protector - A Prospective Randomized Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049457
Enrollment
90
Registered
2023-02-06
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 LMA: Standard anaesthesia protocol will be followed to anaesthetise the patients. 18 G sized cannula will be used to secure the peripheral intravenous line. Pre-oxygenation

Sponsors

Pt.B.D.Sharma University of Health Sciences PGIMS, Rohtak, Haryana
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 90 patients belonging to American Society of Anaesthesiologists(ASA) I or II scheduled for elective surgery under general anaesthesia requiring endotracheal intubation.

Exclusion criteria

Exclusion criteria: Patients having respiratory or pharyngeal pathology, mouth opening 30kg/m2, pregnancy, full stomach, anticipated difficult airway and any patient who refuses to participate in the study will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Success of Intubation through the LMA and comparison between 2 devices - LMA Blockbuster and ProtectorTimepoint: Baseline(T0)-MAP(mmHg),HR(min),spO2(%) After Induction(T1)- MAP(mmHg),HR(min),spO2(%) After Insertion(T2)- MAP(mmHg),HR(min),spO2(%) After Intubation(T3)- MAP(mmHg),HR(min),spO2(%)

Secondary

MeasureTime frame
Success of placement of LMA Time taken for LMA insertion Oropharyngeal Seal pressures Number of attempts and ease of intubation Hemodynamic variations Any special manouvres used Post-operative complicationsTimepoint: Assessment of Mean Arterial Pressures, Heart Rate and Oxygen saturation will be done at Baseline, at Induction, at Insertion of supraglottic device and after Intubation. Post-operative complications-immediately,after half hour and after 1 hour will be assessed. Data compiled and appropriate statistical tests will be applied to analyse the results.

Countries

India

Contacts

Public ContactDr Tavleen Kaur

Pt B D Sharma PGIMS Rohtak

tavleenkaur147@gmail.com9878816667

Outcome results

None listed

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