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To assess how best to give oxygen to patients during attempts of intubation: A randomized controlled trial.

Not Applicable
Conditions
Health Condition 1: 4- Measurement and Monitoring
Registration Number
CTRI/2021/03/032294
Lead Sponsor
All India Institute of Medical Sciences Patna
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients scheduled for General Anaesthesia

ASA I and II

Exclusion Criteria

ASA III/IV

Any history of recent or past respiratory disease

History of presence of nasal pathology

Any anticipated difficult airway defined as:

-Modified Mallampati Grade 3 or 4

-Thyro-mental distance less than 6.5 cm

-Mouth opening less than 4 cm

Patient refusal to take part in the study

Obesity(BMI more than or equal to 30)

Pregnancy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assessment of time taken for saturation to fall to 94% or below, after administering muscle relaxant.Timepoint: Once saturation falls to 94% after administration of muscle relaxant or 10 minutes after giving muscle relaxant, whichever is earlier.
Secondary Outcome Measures
NameTimeMethod
Analyse the arterial carbon dioxide rate of accumulation from baseline till the point when oxygen saturation reaches 94% or at 10 minutes after muscle relaxant administration if saturation remains above 94% throughout.Timepoint: Once saturation falls to 94% after administration of muscle relaxant or at 10 minutes after giving muscle relaxant, whichever is earlier.;Assessment of arterial oxygen partial pressures when arterial haemoglobin saturation reaches 94% or at 10 minutes after muscle relaxant administration if saturation remains above 94% throughout.Timepoint: Once saturation falls to 94% after administration of muscle relaxant or 10 minutes after giving muscle relaxant, whichever is earlier.;Compare PaO2 levels just after preoxygenation i.e. just before IV anaesthetic administration.Timepoint: 5 minutes after start of experiment.
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