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A clinical trail to study the comparison of Proseal Laryngeal Mask Airway versus Endotracheai Tube for Ventilatory Efficacy and Airway Dynamics in Patients Undergoing Beating-Heart Coronary Artery Bypass Grafting.

Comparison of Proseal Laryngeal Mask Airway versus Endotracheal Tube for ventilatory Efficacy and Airway Dynamics in patients Undergoing Beating-Heart Coronary Artery Bypass Grafting in SMS Hospital Jaipur During 2019-2021.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/09/027542
Enrollment
60
Registered
2020-09-02
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: I00-I99- Diseases of the circulatory system

Interventions

Intervention1: Proseal Laryngeal Mask Airway: 30 patients are intubated with Proseal Laryngeal Mask airway then ventilatory efficacy and airway dynamics are noted at different time intervals Intervent

Sponsors

Department of Anaesthesiology SMS Medical CollegeJaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients willing to give written informed consent. 2.Patients with ASA grade II and III 3.Patients of either sex 4.Age groups 40-60 years 5.Weighing 50 to 80 KGS 6.BMI :Less than 40Kg/M.Square

Exclusion criteria

Exclusion criteria: 1.Anticipated difficult intubation/LMA insertion (inadequate mouth opening,cervical spine injury,oropharyngeal pathology) 2.Obese patients(BMI more than 35),COPD patients,Sleep apnea patients 3.Patients having allergy to anaesthetic drugs used in the study 4.REDO and Emergency surgeries

Design outcomes

Primary

MeasureTime frame
To assess and compare peak airway pressure and airway resistance in both groupsTimepoint: Data will be recorded just before induction,1min,3min,5min,15min after induction of device and for every 15min till the end of surgery—

Secondary

MeasureTime frame
1.To determine haemodynamic parameters in both groups 2.To evaluate difference in tidal volume and compliance in both groups 3.To evaluate oxygen saturation and end tidal CO2 4.To evaluate side effects if anyTimepoint: Data will be recorded just before induction,1min,3min,5min,15min after insertion of device and for every 15min till the end of the surgery—

Countries

India

Contacts

Public ContactDR S Bhaskar

Department of Anaesthesiology,SMS Medical College,Jaipur

reemadrrn@gmail.com9413237117

Outcome results

None listed

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