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The effect of inhaled oxygen concentration under general anesthesia on postoperative inflammatory response and cognitive function in patients undergoing laparoscopic urological surgery: a multicenter, randomized controlled trial

The effect of inhaled oxygen concentration under general anesthesia on postoperative inflammatory response and cognitive function in patients undergoing laparoscopic urological surgery: a multicenter, randomized controlled trial

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083065
Enrollment
Unknown
Registered
2024-04-15
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

postoperative cognitive disorder

Interventions

Aged A group:oxygen concentration about 80% under general anesthesia
Aged B group:oxygen concentration about 60% under general anesthesia
Aged C group:oxygen concentration about 40% under general anesthesia
Adult A group:oxygen concentration about 80% under general anesthesia
Adult B group:oxygen concentration about 60% under general anesthesia
Adult C group:oxygen concentration about 40% under general anesthesia

Sponsors

Harbin Medical University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1: Laparoscopic elective surgery patients aged = 18 years old 2: ASA II-III 3: Mechanical ventilation under general anesthesia is required 4: Expected anesthesia time more than 2 hours 5: Obtained informed consent 6: Accessibility to audiovisual communication

Exclusion criteria

Exclusion criteria: 1: Neurological disorders such as acute stroke, Alzheimer's disease, history of neurosurgery surgery, Parkinson's disease, etc 2: Long term use of sedatives, antidepressants, alcoholism, drug dependence, or patients with mental illnesses 3: Severe cardiac insufficiency (NYHA grade III or IV) 4: Severe respiratory insufficiency such as severe COPD or oxygenation index<300 5: Immune deficiency, use of immunosuppressants or glucocorticoids, organ transplantation, etc 6: Pregnant patients 7: Received surgery or mechanical ventilation treatment within two weeks

Design outcomes

Primary

MeasureTime frame
neutrophil-to-lymphocyte ratio, NLR and platelet-lymphocyte ratio, PLR;

Secondary

MeasureTime frame
3-minute Diagnostic Interview for CAM;The Mini Mental State Examination (MMSE);Intraoperative vital signs (rSO2, SpO2, HR, MAP, ETCO2, P-Peak, T, BIS) ;PaO2;The FRAIL Scale;Postoperative cardiovascular complications ; ICU transfer rate;

Countries

China

Contacts

Public ContactHan Fei

Harbin Medical University Cancer Hospital

13895830213@163.com+86 186 8685 7197

Outcome results

None listed

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