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comparing two airway devices that is i gel and baska which one took less time to place in patient throat in general anesthesia

Evaluation and comparison of efficiency of baska mask as supraglotic airway device to i-gel in adult patient undergoing surgery under general anesthesia with contolled ventillation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/03/018182
Enrollment
70
Registered
2019-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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: Baska airway equipment device: EVALUATION AND COMPARISON OF EFFICIENCY OF BASKA MASK AS SUPRAGLOTIC AIRWAY DEVICE TO I-GEL IN ADULT PATIENTS UNDERGOING SURGERY UNDER GENERAL ANAESTHESIA

Sponsors

Dr Mohammed Abdul Majeeth
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients aged between 18 to 60 years. ASA Grade I and II Patients undergoing elective surgical interventions not requiring endotracheal intubation and surgeries lasting for 30-90mins. Those willing to give informed consent Predicted normal airway

Exclusion criteria

Exclusion criteria: age less than 18 and more than 60 years bmi >40 kg/m asa 3 and 4 predicted difficult airway increased aspiration risk full stomach hiatus hernia gastroesophageal reflux disease prone position major head and neck surgery

Design outcomes

Primary

MeasureTime frame
This study is aimed to compare insertion time taken for baska and i-gel. Primary objective Insertion time: It was defined as the time duration between the picking up of the device and itâ??s successful placement by viewing the chest rise after insertion. Timepoint: 4 months

Secondary

MeasureTime frame
Secondary objective 1. The success of insertion- assessed by the number of attempts at insertion 2. Hemodynamic parameters peri- insertion period. Timepoint: 6 months

Countries

India

Contacts

Public ContactDR MOHAMMED ABDUL MAJEETH M

sri ramakrishna hospital

drartirajput4@gmail.com04224500000

Outcome results

None listed

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