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A comparison of two medical airway devices (auragain and igel in patients who will undergo laparoscopic surgery

Comparison of clinical efficacy of Ambu Auragain and I gel in patients undergoing Gynecological Laparoscopic surgeries under General Anesthesia:A comparative study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/041043
Enrollment
100
Registered
2022-03-14
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

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: AMBU AURAGAIN: Ease of insertion No of insertion attempts Oropharyngeal leak pressure Blood staining on removal Post operative sore throat Control Intervention1: IGEL: Ease of insert

Sponsors

Narayana Medical College and Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient with normal investigations and posted for elective laparoscopic Hysterectomy,Cystectomy,Tubectomy ASA Grade 1 and 2 Mallampati Score 1 AND 2 Anticipated duration of surgery <2 Hours

Exclusion criteria

Exclusion criteria: Patients without valid informed consent Patients with predicted difficult airway Patients with high risk of aspiration Patients with respiratory tract pathology or serious bleeding disorder

Design outcomes

Primary

MeasureTime frame
Insertion time Ease of insertion Insertion attempts Oropharyngeal leak pressure soon after insertion and 1 hr after insertion Blood staining on removal Postoperative sore throat Timepoint: 1 minute 5 minutes 10 minutes after device insertion After removal

Secondary

MeasureTime frame
As a conduit for intubation Fiberoptic bronchoscopic grading of device placementTimepoint: 1 minute 5 minutes 1 hour

Countries

India

Contacts

Public ContactVijetha Devaram

Narayana Medical College Hospital

vijethadevaram@gmail.com09440596766

Outcome results

None listed

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