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Effect of continuous positive airway pressure combined with small tidal volume ventilation on lung protection during one-lung ventilation for video assisted thoracoscopic surgery: a prospective randomized controlled study

Effect of continuous positive airway pressure combined with small tidal volume ventilation on lung protection during one-lung ventilation for video assisted thoracoscopic surgery: a prospective randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050888
Enrollment
Unknown
Registered
2021-09-07
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-05-09

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

Conditions

Thoracic disease

Interventions

Group A:Conventional one-lung ventilation
Group B:Continuous positive airway pressure = 2 cmH2O, tidal volume = 40-60 mL
Group C:Continuous positive airway pressure = 5 cmH2O, tidal volume = 60-80 mL

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1. Adult patients aged 18-79 years scheduled for video-assisted thoracoscopic surgery (VATS) with one-lung ventilation for lobectomy under general anesthesia; 2. Agree to participate and sign the informed consent form; 3. ASA (American Society of Anesthesiologists) I-III; 4. Forced expiratory volume in 1 second (FEV1) >= 1.5 L; 5. Body mass index (BMI) 18-28 kg/m^2.

Exclusion criteria

Exclusion criteria: 1. Desaturation below 85%; 2. Intraoperative conversion to thoracotomy; 3. Intraoperative pleural atresia or severe adhesions; 4. Previous history of pneumonectomy and cholecystectomy; 5. Patients with decompensated heart, lung, liver and kidney disease, abnormal coagulation function; 6. Pregnancy and difficult intubation; 7. Patients with severe respiratory diseases or malformations suggested by preoperative imaging data; 8. Patients with severe neuropsychiatric disorders, long-term alcohol, opioid or sedative-hypnotic drug addiction and dependence history.

Design outcomes

Primary

MeasureTime frame
Intrapulmonary shunt(Qs/Qt);PaO2;PaCO2;

Secondary

MeasureTime frame
Field Satisfaction;Postoperative pulmonary complications;

Countries

China

Contacts

Public ContactJia Ke

Affiliated Hospital of North Sichuan Medical College

jieke112221@163.com+86 13990820588

Outcome results

None listed

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