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Comparison of Blockbuster and I gel laryngeal mask airway for safety and efficacy in patients undergoing surgery in general anaesthesia.

Comparison of Blockbuster and I gel laryngeal mask airway for safety and efficacy in patients undergoing surgery in general anaesthesia: A Randomised control Trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058754
Enrollment
74
Registered
2023-10-17
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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: Blockbuster laryngeal mask airway size 3 for 30-50 kg size 4 for 50-70 kg size 5 for 70-100 kg for patient undergoing surgery in general anaesthesia. Control Interventi

Sponsors

Rohilkhand medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult consenting patient of either sex. BMI less than 30 kg/m2 Mallampati classification I & II ASA- I & II Age- 18 to 60 years

Exclusion criteria

Exclusion criteria: Patients’ refusal or inability to give informed consent Patient with neck pathology Anticipated difficult airway Pre-existing cervical spine disease History of gastro-oesophageal reflux or increased risk of Gastric aspiration. Lesion in oral cavity Mouth opening less than 2 cm Loose denture Procedure such as Head & Neck surgery Pregnant females Pre-existing cervical spine disease

Design outcomes

Primary

MeasureTime frame
1.To compare efficacy of Two Laryngeal Mask Airway Devices in terms of •Number of Attempts taken •Time taken for insertion •Haemodynamic parameters like SBP, DBP, MAP, HR. •Ease of Insertion •Oropharyngeal seal pressure 2.To compare the Safety of the Two Laryngeal Mask Airway Devices in terms of •Blood stain on device •Sore throat •Airway trauma Timepoint: Sore throat will be evaluated immediately following surgery, after 30 minutes, two hours, and then every four hours for eight hours—

Secondary

MeasureTime frame
nilTimepoint: nil—

Countries

India

Contacts

Public ContactDr Sarfaraz Ahmad

Rohilkhand medical college and hospital, Bareilly

rinkichandra@yahoo.com8279783945

Outcome results

None listed

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