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A study to compare clinical performance of AMBU AURAGAIN and LMA BLOCKBUSTER in adult patients undergoing general anaesthesia for elective surgeries.

A prospective randomised study Comparing clinical performance of AMBU AURAGAIN and LMA BLOCKBUSTER in adult patients undergoing general anaesthesia for elective surgeries. - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068772
Enrollment
90
Registered
2024-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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: SUPRAGLOTTIC AIRWAY DEVICE Insertion: Group of airway devices that can be inserted into the pharynx to allow ventilation, oxygenation, and administration of anaesthetic gases, without t

Sponsors

Department of Anaesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA grade I and grade II Patients. 2. Age- 18 to 65 years of either sex. 3. Patients undergoing surgery under general anaesthesia. 4. Anticipated normal airway in preanaesthetic evaluation. 5. Posted for surgery requiring supine position only

Exclusion criteria

Exclusion criteria: 1. Patients with anticipated difficult airway 2. Anticipated high risk of aspiration (hiatus hernia, full stomach, pregnancy, gastro-oesophageal reflux). 3. Preoperative respiratory tract infection. 4. Patients with history of allergy or sensitivity to any medication, latex or egg.

Design outcomes

Primary

MeasureTime frame
Oropharyngeal seal pressure(OSP)Timepoint: Once after insertion of supraglottic airway device

Secondary

MeasureTime frame
Ease of insertion of device and gastric tube placementTimepoint: During insertion of device;Hemodynamic parameters (BP, HR, SPO2)Timepoint: Baseline, every 5 minutes for initial 15 minutes and then every 15 minutes till end of the surgery.;Number of attempts takenTimepoint: For successful insertion of device;Post-op complications (Displacement, blood staining, Sore throat, hoarseness, injury)Timepoint: After extubation;Time taken for effective insertionTimepoint: Upto securing the airway

Countries

India

Contacts

Public ContactDr Smriti Garg

LLRM Medical College

swetaanae@gmail.com8750933442

Outcome results

None listed

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