Skip to content

Comparative Effects of Different Ventilator Modes on Pulmonary Microbiota Composition and Postoperative Pulmonary Complications in Patients Undergoing Pulmonary Resection

Comparative Effects of Different Ventilator Modes on Pulmonary Microbiota Composition and Postoperative Pulmonary Complications in Patients Undergoing Pulmonary Resection

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108367
Enrollment
Unknown
Registered
2025-08-28
Start date
2025-08-31
Completion date
Unknown
Last updated
2025-09-01

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

Conditions

Postoperative Pulmonary Complications (PPCs)

Interventions

Pressure-Controlled Ventilation (PCV) group:Pressure-controlled ventilation (PCV) mode was employed during mechanical ventilation.
Volume-Controlled Ventilation (VCV) group:Volume-controlled ventilation (VCV) mode was utilized during mechanical ventilation.

Sponsors

Nanfang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: 1. Voluntary provision of written informed consent 2. Adult patients aged 18-85 years 3. Diagnosis of any of the following conditions: Benign pulmonary tumors; Pulmonary fibrosis; Bronchiectasis; Congenital lung diseases; Severe chronic obstructive pulmonary disease (COPD; GOLD stage 3-4); Traumatic lung injury; Chronic pulmonary embolism 4. Scheduled for elective pulmonary resection under general anesthesia with anticipated one-lung ventilation duration =60 minutes 5. ASA physical status classification I-III

Exclusion criteria

Exclusion criteria: 1. History of acute lung injury (ALI) prior to surgery 2. Acute respiratory distress syndrome (ARDS) or respiratory failure within the past 3 months 3. Severe comorbidities, including: Advanced liver dysfunction (e.g., hepatic failure or Child-Pugh class B/C) 4. Chronic kidney disease with glomerular filtration rate (GFR) II) 6. Poorly controlled asthma or FEV1% <60% predicted 7. Investigator-determined ineligibility based on: Collected baseline data (age, sex, BMI, medical history, medication use); Overall assessment of suitability for study participation

Design outcomes

Primary

MeasureTime frame
Incidence of Adverse Events;Hemodynamic Changes and Postoperative Pain Scores;Oxygenation Index at Different Perioperative Time Points;Graded assessments performed via chest radiography and routine laboratory tests on postoperative day (POD) 2 or 3, and when any pulmonary complications were clinically suspected.;Duration of Mechanical Ventilation Weaning;Incidence of Postoperative Pulmonary Complications (PPCs) During the First Week, Including Comprehensive Outcome Analysis and Individual PPCs Analysis;

Secondary

MeasureTime frame
Cardiac tissue and plasma/urine biomarkers, including sCD40L, NT-proBNP, BNP, creatinine, and lipid profiles;Length of Stay in ICU/Intermediate Care Unit and Time to Discharge;Incidence of Postoperative Extrapulmonary Complications (PEPCs) During the First Week;Incidence of Pulmonary Complications Occurring Between Postoperative Days 7-30;Major In-Hospital Cardio- or Cerebrovascular Events (e.g., mortality, stroke, myocardial infarction, heart failure) and Acute Kidney Injury (AKI);

Countries

China

Contacts

Public ContactLiu Kexuan

Nanfang Hospital, Southern Medical University

2235912752@qq.com+86 137 1068 4096

Outcome results

None listed

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