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Comparison of the effectiveness of two supraglottic airway devices AmbuÃ?® AuraGainââ??¢ laryngeal mask airway with LMA ProSeal ââ??¢ in patients undergoing laparoscopic surgeries.

A randomised clinical trial comparing the effectiveness of AmbuÃ?® AuraGainââ??¢ laryngeal mask airway with LMA ProSeal ââ??¢ in patients undergoing laparoscopic surgeries.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012836
Enrollment
80
Registered
2018-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: - Health Condition 2: null- ASA physical status I and II patients scheduled for laparoscopic surgeries

Interventions

Intervention1: AmbuÃ?® AuraGainââ??¢ laryngeal mask airway: new second generation Supraglottic airway device Control Intervention1: LMA ProSealââ??¢: second generation Supragottic airway device

Sponsors

SDM Medical collegeDharwad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients who are undergoing elective laparoscopic surgeries 2.Age:18-65years 3.ASA physical status I and II 4.Those willing to participate

Exclusion criteria

Exclusion criteria: 1.Patient refusal 2.ASA physical status III and IV 3.Obesity BMI >30 kilograms per meter square 4.Pregnancy 5.High risk of pulmonary aspiration , inadequate fasting, gastro-esophageal reflux disease (GERD) �Restricted mouth opening

Design outcomes

Primary

MeasureTime frame
Oropharyngeal leak pressure and mucosal pressure Timepoint: Oropharyngeal leak pressure and mucosal pressure in cm of water at insertion,after pneumoperitonium,at 30,60,90,120 minutes

Secondary

MeasureTime frame
Number of insertion attemptsTimepoint: 1,2,3;Time required for insertionTimepoint: seconds

Countries

India

Contacts

Public ContactDr Archana Bharadwaj

SDM medical college

archana.a.b16@gmail.com9886468625

Outcome results

None listed

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