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A clinical trial to comparatively evaluate peak inspiratory pressure and dynamic compliance between ambu auragain laryngeal mask airway and endotracheal tube

Comparison of peak inspiratory pressure and dynamic compliance between ambu auragain laryngeal mask airway and endotracheal tube - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071479
Enrollment
70
Registered
2024-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: K80-K87- Disorders of gallbladder, biliary tract and pancreas

Interventions

Intervention1: Ambu AuraGain: Patients in Group A will be given Ambu Auragain to secure the airway. Control Intervention1: Endotracheal tube: Patients in Group E will be given Endotracheal tube to sec

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults of either gender 2. Age between 18 to 65 years 3. Patients undergoing elective laparoscopic cholecystectomy 4. American Society of Anaesthesiologists Physical Status (ASA) I, II and III patients 5. BMI less than 35 kg/m2

Exclusion criteria

Exclusion criteria: 1. Anticipated anatomical or physiological difficult airway 2. Pregnant patients 3. Presence of significant acute or chronic lung disease 4. Presence of significant acute or chronic cardiac disease 5. Patient refusal to participate in study

Design outcomes

Primary

MeasureTime frame
Change in peak inspiratory pressure and dynamic compliance with the use of either Ambu AuraGain or endotracheal tube .Timepoint: Patients will be observed at baseline after induction of anaesthesia , 5 minutes after positioning of patient and before pneumoperitoneum , 5 minutes post pneumoperitoneum creation ,10 minutes post pneumoperitoneum and then every 10 minutes upto 180 minutes after induction of anaesthesia—

Secondary

MeasureTime frame
Change in haemodynamic parameters ,ease of insertion of airway device & post operative complications if any with the use of airway device whether Ambu AuraGain or endotracheal tube.Timepoint: Patients will be observed at baseline, immediately after insertion, at 5 minutes,10 minutes,20 minutes,30 minutes & then every 15 minutes upto 180 minutes after induction of anaesthesia.Post operative complications will be recorded till the discharge of the patient from the post anaesthesia care unit.—

Countries

India

Contacts

Public ContactDr Abhideep Singh Sandhu

Dayanand Medical College and Hospital

singhabhideep10@gmail.com8968828829

Outcome results

None listed

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