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Chest Infection After Surgery With Two Different Amount Of Oxygen.

Post-Operative Pulmonary Complications With High FiO2 Or Standard FiO2 In Adult Patients Undergoing Abdominal Surgery: A Non-Inferiority Trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/041290
Enrollment
224
Registered
2022-03-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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: High FiO2(0.8): Inra-Operative high FiO2 will be used throughout the surgery. Duration:from start of surgery till the end. Control Intervention1: Standard FiO2(0.3-0.4): Standard FiO2 o

Sponsors

Dr Souvik Maitra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients (aged between 18 years and 75 years) of American Society of Anesthesiologists physical status I or II, of either sex undergoing elective or emergency abdominal surgery with duration more than 2 hours under general anesthesia will be recruited in this study

Exclusion criteria

Exclusion criteria: 1. Patients refusal to participate in the study 2. Patients undergoing emergency laparotomy for trauma and related causes. 3. Known COPD or other chronic lung diseases 4. Preoperative diagnosis of Pneumonia 5. Known deformity of chest wall or thoracic spine 6. Pre-existing significant cardiac, renal and hepatic diseases 7. Intraoperative massive blood loss (defined by blood loss >40 ml/kg) or massive transfusion (more than 8 unit of PRBC transfusion during surgery) 8. Patients with history of previous thoracic surgery. 9. BMI > 30 kg/m2, 10. Patients who are on high dose of vasopressors (defined as noradrenalin 10mcg/m or equivalent)

Design outcomes

Primary

MeasureTime frame
The primary objective of this study is to identify whether High FiO2 with PEEP titration is Non-Inferior to standard FiO2 in terms of incidence of POPC up to 5 days after surgery.Timepoint: Postoperative day 3 & 5

Secondary

MeasureTime frame
. Platelet- neutrophil ration and neutrophil- lymphocyte ratioTimepoint: Post-Operative day1;1. SpO2 at room airTimepoint: one hour post-surgery and after 24 hours;Days alive without antibioticTimepoint: Day 28;Duration of hospital stayTimepoint: At hospital discharge;Surgical site infectionTimepoint: Postoperative day 5 or hospital discharge

Countries

India

Contacts

Public ContactDr Jose Cyriac kochupurackal

AIIMS

souvikmaitra@live.com8146727891

Outcome results

None listed

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