Proseal LMA Insertion using introducer tool and suction catheter in childre

Not Applicable

• Conditions: Health Condition 1: null- Healthy paediatric patients ASA I and II for elective surgeries

• Registration Number: CTRI/2018/04/013012
• Lead Sponsor: Vijayanagar Institute of Medical Sciences

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: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

Posted for elective surgeries between 5-30 Kg,ASA I and II

After induction of general anaesthesia, Proseal is inserted as per the allocation and the parameters are noted.

Exclusion Criteria

Patients with known or predicted difficult airway or patients at risk of aspiration.

Presence of significant co-morbidities or recent or active respiratory tract infection.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The ease of insertion (number of attempts and time taken to provide an effective airway with first attempt success rate of insertionTimepoint: The Primary Outcome Parameter is assessed after pLMA insertion in two groups, at <br/ ><br>1min,2min,3min,4min,5min, or max. 3 attempts of insertion <br/ ><br>

Secondary Outcome Measures

Name	Time	Method
Efficacy of airway seal. Any episodes of desaturation (SpO2 90 %) or other adverse events. <br/ ><br> <br/ ><br>Heart rate and BP changes before, during and after insertion. <br/ ><br>Any visible blood staining on suction catheter, laryngoscope / PLMAâ?¢ noted at removal. <br/ ><br>Any trauma to mouth, lips and tongue. <br/ ><br>After 18-24 hrs postoperatively, patients or parents were asked about sore throat (constant pain even without swallowing), dysphonia (difficulty or pain on speaking), dysphagia (difficulty or pain on swallowing). <br/ ><br>Timepoint: Upto 24 h post operatively