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Comparing the effect of two different flow rates of high flow nasal cannula on increasing the oxygen content of blood during the start of general anaesthesia.

Comparison of apnoeic oxygenation efficiency using high flow nasal cannula at two different flow rates in patients posted for surgery under general anaesthesia - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/067510
Enrollment
56
Registered
2024-05-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: HFNC flow of 40L/min for 3 minutes during apnoeic oxygenation.: During induction of general anaesthesia, preoxygenation will be done at 40 L/min flow rate using High Flow Nasal Cannula

Sponsors

Maulana Azad Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I and II

Exclusion criteria

Exclusion criteria: Any known contraindication to HFNC: bleeding in nose or oropharynx, pre-existing nasal obstruction, greater than 50 percent of nares occluded by nasal prongs. Patients on oxygen therapy. Any underlying chronic or restrictive lung disease (kyphoscoliosis, burn contractures). Previous lung surgery. BMI greater than 35 kg per meter square. Planned for awake intubation or a difficult airway. Any contra-indication to continuous positive airway pressure (CPAP) treatment. Pregnant patients, autonomic neuropathy, history of gastro-esophageal reflux disease(GERD).

Design outcomes

Primary

MeasureTime frame
PaO2 in both the groups.Timepoint: At the end of 3 minutes of apnoeic oxygenation

Secondary

MeasureTime frame
Mean difference in PaO2 and PaCO2 levels in both groups (baseline, after 3 minutes of pre-oxygenation, after 3 minutes of apnoeic oxygenation) . End tidal oxygen (FETO2) and End tidal carbon dioxide (ETCO2) after securing a definitive airway and after 3 minutes. Percentage of population with hypoxemia (SpO2 less than 92%). Patient comfort during pre-oxygenation immediately before induction on a 5 point Likert scale.Timepoint: Baseline, after 3 minutes of pre-oxygenation, after 3 minutes of apnoeic oxygenation, after securing a definitive airway and after 3 minutes of securing a definitive airway.

Countries

India

Contacts

Public ContactNitya Nyalakonda

Maulana Azad Medical College

monaarya@hotmail.com9021643760

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026