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Influence of different modes of oxygen therapy on lung outcome after spine surgery:A study

Influence of high flow nasal cannula vs. conventional oxygen therapy on pulmonary outcome after spine surgery:A randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041803
Enrollment
64
Registered
2022-04-11
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

Health Condition 1: S340- Concussion and edema of lumbar andsacral spinal cord

Interventions

Intervention1: High flow nasal cannula and Conventional oxygen therapy: Group A will receive HFNC therapy 0.4 FiO2 at 40 lpm for next 3 hours after extubation. Group B patients will receive conventi

Sponsors

Postgraduate Institute of Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Spine instrumentation for trauma and /or any pathology below fifth thoracic vertebra in prone position under GA. ASA I to III physiological status.

Exclusion criteria

Exclusion criteria: Patient refusal. Obesity( BMI >30). known case of respiratory disease including bronchial asthma,COPD,TB,pneumonia. Inability to keep arterial oxygen saturation above 94% without supplemental oxygen. Paitent with blunt trauma chest and severe brain injury. Patient with prior endotracheal and/or chest drain tube.

Design outcomes

Primary

MeasureTime frame
To compare PaO2/FiO2 ratio at the end of three hours of oxygen therapy in between group A(HFNC 0.4 FiO2,40lpm),and group B(venturi mask 0.4 FiO2,10 lpm)following thoraco-lumbar spine surgery.Timepoint: baseline, immediate postoperative period, 3hrs, 6hrs and 24 hr

Secondary

MeasureTime frame
To compare the changes in P/F ratio,lactate values,lung ultasound scores at different time intervals,to compare the physiological variables like heart rate,respiratory rate,mean arterial pressure in post operative period,to observe any adverse events like PONV,SSI in postoperative period,to konw the comprison of incidences of patients developing clinically relevant postoperative hypoxaemia during study period in between groups.Timepoint: Pre intubation(baseline),at the end of surgery,3 hrs,6hrs,24 hrs after surgery in between the groups

Countries

India

Contacts

Public ContactDr Shyam Charan Meena

Post Graduate Institute of Medical Education and Research

drshyam.pgi@gmail.com7891669817

Outcome results

None listed

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