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The impact of different inhaled oxygen concentrations on early postoperative oxygenation in obese patients

The impact of different inhaled oxygen concentrations on early postoperative oxygenation in obese patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112785
Enrollment
Unknown
Registered
2025-11-19
Start date
2025-07-29
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

Obesity

Interventions

FiO2 40% group (L group):After intubation during the perioperative period, mechanical ventilation was used to inhale an oxygen concentration of 40% until the tracheal tube was removed.
FiO2 60% group (M group):After intubation during the perioperative period, mechanical ventilation was used to inhale an oxygen concentration of 60% until the tracheal tube was removed.
FiO2 80% group (H group):After intubation during the perioperative period, mechanical ventilation was used to inhale an oxygen concentration of 80% until the tracheal tube was removed.

Sponsors

The First Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18 to 45 years old; 2. ASA (American Society of Anesthesiologists Classification) grades II-III; 3. Body mass index (BMI) 35-45kg/m^2; 4. Patients undergoing elective laparoscopic sleeve gastrectomy; 5. No history of drug allergies or abnormal anesthesia; 6. Preoperative blood oxygen saturation ?=94%; 7. Plan to remove the tracheal tube in the operating room.

Exclusion criteria

Exclusion criteria: 1.Patients with a history of ALI/ARDS within 3 months; 2. Patients with blood oxygen saturation<94% without oxygen inhalation before surgery; 3. Severe pulmonary dysfunction and severe chronic obstructive pulmonary disease patient; 4.Patients with severe cardiac dysfunction (preoperative LVEF<30% or NYHA grade IV); 5. Severe liver dysfunction (Child Pugh C grade); 6. Patients with severe renal dysfunction (undergoing dialysis before surgery); 7. Patients who plan to be transferred to the ICU after surgery; 8. Refusal to join clinical trials.

Design outcomes

Primary

MeasureTime frame
Oxygenation index 30 minutes after extubation following surgery;

Secondary

MeasureTime frame
Arterial blood gas measurements at 5 min after room entry, 30 min after extubation, and 24 h postoperatively;Percentage area of Central Ventilation (CoV), Dependent Stable Zone (DSS), and Non-dependent Stable Zone (NSS) during EIT monitoring at 5 min after room entry and 30 min after extubation;Hemodynamic parameters: Heart rate (HR), Mean arterial pressure (MAP), Systolic blood pressure (SBP);The total intraoperative doses of neuromuscular blocking agents, opioids, and cyclopropofol were recorded.;

Countries

China

Contacts

Public ContactGuo Qiongmei

The First Hospital of Hebei Medical University

guo-qiongmei@163.com+86 155 1166 0729

Outcome results

None listed

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