Comparison between two airway devices i-gel vs Laryngeal mask airway-unique on easiness of insertion during general anaesthesia

Not Applicable

Completed

• Conditions: Health Condition 1: null- Anaesthesia

• Registration Number: CTRI/2011/11/002168
• Lead Sponsor: Government medical college Thiruvananthapuram

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 20

Inclusion Criteria

ASA 1 - Healthy patient without organic, biochemical, or psychiatric disease

ASA 2 - A patient with mild systemic disease, e.g., mild asthma or well-controlled hypertension. No significant impact on daily activity. Unlikely to have an impact on anesthesia and surgery

Exclusion Criteria

ASA 3- Significant or severe systemic disease that limits normal activity, e.g., renal failure on dialysis or class 2 congestive heart failure. Significant impact on daily activity. Probable impact on anesthesia and surgery

ASA 4-Severe disease that is a constant threat to life or requires intensive therapy, e.g., acute myocardial infarction, respiratory failure requiring mechanical ventilation. Serious limitation of daily activity. Major impact on anesthesia and surgery

ASA 5-Moribund patient who is equally likely to die in the next 24 hours with or without surgery

ASA 6-Brain-dead organ donor

Duration of surgery more than 2 hours

Emergency surgery

Surgery in positions other than supine

Pathology of neck or upper repiratory tract

Potential difficult intubation

Mouth opening less than 2.5 cms

Pregnant women

BMI more than 35 kg/m2

Patients with reported hypersensitivity for one or more medications and latex

Increased risk of aspiration ( hiatus hernia , gastro esophageal reflux , full stomach )

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of insertionTimepoint: Time from picking up the device to first successful breath made by manual ventilation

Secondary Outcome Measures

Name	Time	Method
Hemodynamic effectsTimepoint: Pulse Rate , Blood Pressure (systolic , diastolic & mean) , Oxygen saturation are monitored and recorded.;Leak volumesTimepoint: The difference between inspired tidal volume (ITV) and expired tidal volume (ETV);Number of insertion attemptsTimepoint: A failed attempt is defined as removal of the device from the mouth before re-insertion.;Perioperative ComplicationsTimepoint: Bronchospasm ,Laryngospasm and coughing , trauma , postoperative sore throat (constant pain, independent of swallowing), dysphagia (difficulty or pain with swallowing), dysphonia (difficulty or pain with speaking);Reposition attemptsTimepoint: Manipulations allowed: gentle pushing or pulling of the device, chin lift, jaw thrust, head extension, or neck flexion.;Sealing pressure (airway leak pressure)Timepoint: Measuring the minimal airway pressure at which an audible gas leak occurred using a stethoscope placed just lateral to thyroid cartilage.