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Clinical Trials/NCT07372378
NCT07372378Not yet recruitingNot Applicable

Association of Various Introperative Tidal Volumes and Postoperative Pulmonary Complications After Video-assisted Thoracic Surgery

First Affiliated Hospital of Zhejiang University0 sites650 target enrollmentStarted: January 20, 2026Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
650
Primary Endpoint
Postoperative Pulmonary Complications (PPCs)

Study Overview

Brief Summary

The incidence of lung cancer in China is increasing year by year. Currently, the treatment primarily based on video-assisted thoracoscopic surgery (VATS) is still considered the optimal approach for early-stage non-small cell lung cancer. The widespread application of traditional one-lung ventilation (OLV) technology not only achieves effective lung isolation, but also facilitates exposure of the surgical field during thoracoscopic surgery, making it more convenient for surgeons to operate. However, the occurrence of hypoxemia during one-lung ventilation may pose a risk to patient safety.

One-lung ventilation can lead to increased intrapulmonary shunt, ventilation/perfusion (V/Q) mismatch, and ischemic-hypoxic lung injury. Hypoxemia is the major problem during one-lung ventilation. Postoperative pulmonary complications (PPCs) are among the major complications following thoracic and general anesthesia surgeries, including atelectasis, pneumonia, and respiratory failure, which significantly prolong hospital stay and increase mortality.

Low tidal volume lung-protective ventilation strategies have been widely implemented. Additionally, permissive hypercapnia, reducing peak airway pressure to minimize barotrauma, and decreasing FiO₂ all help reduce pulmonary complications.Recently, researchers have focused on optimizing ventilation strategies during OLV, such as using PEEP or low VT ventilation alone or in combination, or exploring different combinations of tidal volume and respiratory frequency under consistent minute ventilation (VE), aiming to balance lung protection and oxygenation, reduce complications, and improve patient outcomes.

However, to date, there is still no gold standard tidal volume ventilation strategy for reducing pulmonary complications in patients undergoing lung resection.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
51 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age > 50 years.
  • ASA physical status I-II.
  • The cardiopulmonary and other vital organ functions are basically normal, and the patient is able to tolerate surgery.
  • Ariscat score >
  • Informed consent has been obtained.

Exclusion Criteria

  • Patients who refuse to participate in the clinical trial, or have cognitive impairment or impaired ability to understand and express themselves.
  • ASA physical status ≥ III.
  • Patients with congestive heart failure, severe aortic stenosis, or extensive pleural adhesions.
  • Patients with severe psychiatric disorders or allergy to anesthesia-related medications.
  • Patients with severe organ dysfunction such as the liver or kidney dysfunction.

Outcomes

Primary Outcomes

Postoperative Pulmonary Complications (PPCs)

Time Frame: 1-7 days after surgery

Postoperative Pulmonary Complications (PPCs): Incidence of any PPC within 7 days postoperatively

Secondary Outcomes

  • Incidence of hypoxemia(during surgery)
  • Length of Hospital Stay(through study completion, an average of 1 year)

Investigators

Sponsor
First Affiliated Hospital of Zhejiang University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

xiangming fang

Professor

First Affiliated Hospital of Zhejiang University

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