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se of a new monitor to compare two different anaesthesia induction techniques

Not Applicable
Completed
Conditions
Health Condition 1: K928- Other specified diseases of the digestive system
Registration Number
CTRI/2018/12/016761
Lead Sponsor
Seth GSMC and KEM Hospital Diamond Jubilee Society Trust
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

1) ASA physical status 1 or 2

2) Children in whom rapid sequence induction is planned and indicated (those with full stomach such as intestinal obstruction)

3) Children with preoperative SpO2 of greater than 95% on room air

Exclusion Criteria

1) Children with anticipated difficult airway

2) Children with haemodynamic instability

3) Children with dyshaemoglobinemias

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare ultra-modified rapid sequence induction with a modified rapid sequence induction with respect to the trends in the oxygen reserve indexTM in children <br/ ><br>Timepoint: 0, 2, 3, 4 minutes after starting induction technique
Secondary Outcome Measures
NameTimeMethod
To compare the incidence of desaturation and time to desaturation if at all in the two groupsTimepoint: 0, 2, 3, 4 minutes after starting induction technique
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