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Observational study comparing the safety and efficacy of Igel Supraglottic airway device insertion in anaesthetised patients by Anesthesia faculty versus residents

Observational study comparing the safety and efficacy of Igel Supraglottic airway device insertion in anaesthetised patients by Anesthesia faculty versus residents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/12/038679
Enrollment
60
Registered
2021-12-16
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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: I-Gel insertion by faculty: 15 minutes Control Intervention1: I-Gel insertion by residents: 15 minutes

Sponsors

Department of Anesthesiology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA grade I-II fit patients. 2. Patients posted for elective surgery under GA requiring I-gel Supraglottic Airway device insertion. 3. Availability of informed consent and willingness of the patient to be a part of the study.

Exclusion criteria

Exclusion criteria: 1. Patients belonging to ASA grade III-IV 2. Patients with cardiac, neurological and respiratory diseases. 3. Patients with full stomach. 4. Emergency case patients. 5. Patients scheduled for head and neck surgery

Design outcomes

Primary

MeasureTime frame
To observe the haemodynamic parameters at the time of Igel insertionTimepoint: 5 minutes

Secondary

MeasureTime frame
To compare the number of attempts taken for successful insertion of i-gel as well as the time taken to do so by each group. Timepoint: 5 minutes;To observe any complications during and after the insertion. Timepoint: 20 minutes

Countries

India

Contacts

Public ContactDr Dipanjali Mahanta

Dr. D.Y. Patil Medical College and Hospital and Research Centre, Pimpri Pune

dipanjalimahanta@gmail.com9673586122

Outcome results

None listed

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