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The mechanism of sevoflurane in alleviating acute lung injury induced by one-lung ventilation

The mechanism of sevoflurane in alleviating acute lung injury induced by one-lung ventilation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065614
Enrollment
Unknown
Registered
2022-11-10
Start date
2022-11-22
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

acute lung injury

Interventions

Control Group:Propofol combined with dexmedetomidine was continuously pumped intravenously
Experimental group:Sevoflurane inhalation combined with dexmedetomidine intravenously
Experimental group:Sevoflurane inhalation anesthesia
Control Group:Propofol was continuously pumped intravenously

Sponsors

the First Affiliated Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing segmental or lobectomy; 2. ASA I-II, age 18-65 years old, BMI: 18.5-28kg/m^2; 3. Patients without preoperative respiratory dysfunction and cardiovascular and cerebrovascular underlying diseases; 4. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who received radiotherapy, chemotherapy and immunotherapy within one month before surgery; 2. Patients with severe hypertension and those using angiotensin-converting enzyme inhibitor antihypertensive drugs with severe cardiovascular disease before surgery New York Heart Association (NYHA) class II and above; 3. Patients with abnormal liver and kidney function before surgery; 4. Those with fever or infection before surgery; 5. Patients with preoperative respiratory disease (COPD asthma pneumonia pulmonary edema history of pulmonary surgery); 6. Long-term smoking and drinking, those with cardiovascular and cerebrovascular diseases, metabolic diseases, and autoimmune diseases; 7. Have a history of narcotic and analgesic drug abuse and a history of mental and neurological diseases; 8. Those who have difficulty maintaining SPO2 above 95% during anesthesia; 9. Intraoperative estimated blood loss of more than 500ml or intraoperative blood transfusion and intraoperative hemodynamics difficult to maintain stable.

Design outcomes

Primary

MeasureTime frame
Partial arterial oxygen pressure;interleukin-6;Tumor necrosis factor-a;Tight junction protein;Glutathione;malondialdehyde;Glutathione peroxidase 4;Superoxide dismutase;The changes of lung histopathological ;

Secondary

MeasureTime frame
Pulmonary complications;

Countries

China

Contacts

Public ContactLinjia Zhu

The First Affiliated Hospital with Nanjing Medical University

zhulinjia2010@163.com+86 13813972121

Outcome results

None listed

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