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Effects of different oxygen concentration during the recovery period before extubation after general anesthesia on hypoxemia after extubation in postanesthesia care unit

Effects of different oxygen concentration during the recovery period before extubation after general anesthesia on hypoxemia after extubation in postanesthesia care unit

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112837
Enrollment
Unknown
Registered
2025-11-20
Start date
2025-11-20
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Hyoxemia

Interventions

Control group:FiO2 will be set at 100% immediately after arriving at PACU after surgery until extubation.
Trial group:FiO2 will be set at 30% immediately after arriving at PACU after surgery until extubation.

Sponsors

The Sixth Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18–65 years scheduled for elective abdominal surgery in the supine position 2. ASA physical status I–III 3. Cardiac function class 1–2 4. BMI between 18 kg/m^2 and 28 kg/m^2 5. SpO2 >= 94% on room air 6. Pre-anesthesia assessment predicts no anticipated difficulty with airway management, mask ventilation, tracheal intubation, or extubation

Exclusion criteria

Exclusion criteria: 1. Recent respiratory tract infection, with preoperative chest CT showing atelectasis, pulmonary inflammation, pulmonary fibrosis, pleural effusion, etc. 2. History of thoracic surgery, or concomitant thoracic or other surgical procedures; or presence of sternum or rib fractures, chest deformity, difficulty raising both upper limbs, or scoliosis 3. Presence of gastrointestinal obstruction or high risk for reflux and aspiration, such as pregnant patients 4. History of significant organ dysfunction, such as chronic kidney disease, heart failure, hepatic insufficiency, or mobility impairment 5. Intraoperative occurrence of allergic reactions, massive hemorrhage, or suspected pulmonary embolism, pulmonary edema, or myocardial injury 6. Currently participating in other clinical studies that may interact with this study 7. Psychiatric abnormalities or cognitive impairment, leading to poor cooperation (e.g., severe auditory or visual impairment, intellectual disability, or low educational level preventing comprehension of study materials)

Design outcomes

Primary

MeasureTime frame
Incidence of hypoxemia (SpO2 < 90%) from extubation to leaving the post-anesthesia care unit (PACU);

Secondary

MeasureTime frame
Incidence of pulmonary-related complications within 7 days after surgery;Arterial partial pressure of oxygen (PaO2), alveolar-arterial oxygen partial pressure difference (AaDO2), and estimated venous admixture (EVA) after tracheal extubation;Incidence of severe hypoxemia from extubation to leaving the post-anesthesia care unit (PACU);Score of lung ultrasound after extubation;Area of atelectasis shown on chest CT after extubation;Unplanned transfers to the ICU after surgery;Length of postoperative stay;Readmissions within 30 days after surgery;All deaths within 30 days after surgery;Number of adverse events related to heart, brain, kidneys, or liver 30 days after surgery;

Countries

China

Contacts

Public ContactJin Sanqing

The Sixth Affiliated Hospital, Sun Yat-sen University

jinsq@mail.sysu.edu.cn+86 137 1936 6863

Outcome results

None listed

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