Effect of Different Inspired Oxygen Concentrations on Intraoperative Recruitment Outcomes in Patients Undergoing Abdominal Surgery

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study intends to evaluate the effect of different inhaled oxygen concentrations on the effect of lung recruitment in patients undergoing abdominal surgery. During perioperative mechanical ventilation, higher FiO2 is usually given to prevent the occurrence of hypoxemia, but there are no conclusions about the setting of optimal FiO2 during surgery. Dynamic pulmonary compliance enables real-time monitoring of alveolar changes and is used to assess pulmonary function in intraoperative patients. The value of compliance represents the number of air-containing alveoli; the more alveoli are trapped, the less air-containing tissue there is and the lower the compliance. Lung recruitment, as part of a lung-protective ventilation strategy, is effective in opening alveoli and improving oxygenation. This single-center, randomized controlled trial will explore the optimal inspired oxygen concentration that allows patients to benefit from lung recruitment and the duration of improvement in lung compliance after lung recruitment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 64
Healthy Volunteers: f
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• ASA physical status classification: I or II.

• Adults aged 18 to 64 years, regardless of gender.

• BMI between 18 kg/m² and 25 kg/m².

• Patients undergoing elective abdominal surgery under general anesthesia.

• Patients with estimated operating time ≥1.5h and intraoperative bleeding ≤500ml.

• Patients who have provided written informed consent after understanding the study purpose, procedures, and potential risks.

Locations
Other Locations
China
Northern Jiangsu People's Hospital
RECRUITING
Yangzhou
Contact Information
Primary
Ju GAO
doctor2227@163.com
18051063988
Time Frame
Start Date: 2025-04-01
Estimated Completion Date: 2026-01-31
Participants
Target number of participants: 88
Treatments
Experimental: A: FiO2 = 30%
FiO2 of group A = 30%. If SPO2 \< 94%, improve FiO2; if FiO2≥40%, eliminate the patient.
Experimental: B: FiO2=40%
FiO2=40%
Experimental: C: FiO2=60%
FiO2=60%
Experimental: D: FiO2=80%
FiO2=80%
Related Therapeutic Areas
Sponsors
Leads: Northern Jiangsu People's Hospital

This content was sourced from clinicaltrials.gov