A study comparing different methods for filling the lungs with maximal oxygen before introducing a tube into the windpipe in patients who needs that to be done rapidly.
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2019/01/017248
- Lead Sponsor
- Jubilee Mission Medical College and research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
All adult patients requiring Rapid Sequence Induction for surgical procedures will be included.
. 18-80 years of age
. Informed consent
Exclusion Criteria
. Contraindications for bag mask or HFNO (Faciomaxillary Injury , Nasal Bleed ,Nasal pack )
. Pregnancy
. Suspected or known difficult airway (Mallampati class 3 or 4,or Cormack-Lehane grade 4 recorded during previous intubation procedures)
. BMI more than 35
. Patients who fail to maintain a saturation of 95% after pre-oxygenation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The incidence of patients with SPO2 less than 93% during intubation in HFNO and Bag mask group. <br/ ><br>It is measured from induction of anaesthesia until 1 min after intubation whereafter the protocol was ended.Timepoint: 18 months
- Secondary Outcome Measures
Name Time Method .Mean lowest SPO2 during intubation. <br/ ><br>.Median intubation time <br/ ><br>.Median apnoea time <br/ ><br>.Number of laryngoscopy attemptsTimepoint: 18 months