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The Impact of Regular Lung Recruitment Maneuvers on Postoperative Pulmonary Complications in Patients Undergoing Robot-Assisted Lung Resection

The Impact of Regular Lung Recruitment Maneuvers on Postoperative Pulmonary Complications in Patients Undergoing Robot-Assisted Lung Resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128686
Enrollment
Unknown
Registered
2026-07-24
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Postoperative pulmonary complications: pneumonia

Interventions

Control Group (Periodic Lung Recruitment Maneuvers Group):Periodic Mechanical Lung Recruitment Maneuver
Experimental Group (No Periodic Lung Recruitment Maneuvers Group):No Periodic Lung Recruitment Maneuvers

Sponsors

The Fifth Affiliated Hospital, Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign the informed consent form; 2. ASA Physical Status Classification of I to III; 3. Aged 18 to 75 years, regardless of gender; 4. BMI between 18 and 30 kg/m^2; 5. Patients scheduled to undergo elective robot-assisted lobectomy/segmentectomy/wedge resection under general anesthesia with bronchial intubation, and for whom one-lung ventilation is anticipated to last for 60 minutes or longer.

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating patients; 2.Patients with acute or chronic respiratory failure, chronic obstructive pulmonary disease (COPD), poorly controlled asthma, or acute respiratory distress syndrome (ARDS); 3.Severe cardiovascular complications (defined as NYHA Class III to IV heart failure, acute coronary syndrome, or sustained ventricular tachycardia); 4.Contraindications to lung recruitment maneuvers, such as: hemodynamic instability, pulmonary bullae, bronchopleural fistula, undrained pneumothorax, severe barotrauma, severe pulmonary edema, elevated intracranial pressure, etc. 5.History of mechanical ventilation within the past 15 days; 6.Previous history of pulmonary resection surgery; 7.Patients with uncontrolled anxiety, schizophrenia, or other psychiatric disorders; 8.Participation in another interventional study with similar primary outcomes;

Design outcomes

Primary

MeasureTime frame
Pneumonia;Acute Respiratory Distress Syndrome (ARDS);Atelectasis;Pleural Effusion;Bronchospasm;Respiratory Failure;Pneumothorax;Aspiration Pneumonitis;

Secondary

MeasureTime frame
Oxygenation Parameters;Chest Tube Removal Time;Cardiac Complications;QoR-15;Time to Tracheal Extubation and PACU Observation Time;Infectious Complications;Visual Analog Scale (VAS);Length of Hospital Stay (LOS);

Countries

China

Contacts

Public ContactShanShan Ou

The Fifth Affiliated Hospital, Sun Yat-Sen University

san332009@163.com+86 756 252 8355

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026