Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT06644066

Partial Pressure of Oxygen Control Method in Identification of Intersegmental Plane

Led by Tang-Du Hospital · Updated on 2025-01-07

60

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In recent years, an increasing number of pulmonary nodules have been detected through CT screening. The traditional surgical method for lung cancer is lobectomy combined with lymph node dissection. However, recent studies have demonstrated that sublobar resection for early non-small cell lung cancer (NSCLC) is an effective alternative with the additional benefit of preserving more pulmonary function. However, it also faces many problems, the most prominent of which is the rapid and accurate identification of the intersegmental plane (ISP) during surgery. The modified inflation-deflation method for identifying the ISP is the most commonly used method in anatomical sublobar resection. Nevertheless, the lengthy waiting periods and the lack of clear delineation represent significant challenges in clinical practice. The Partial pressure of Oxygen Control method facilitates the efficient determination of the ISP by reducing the oxygen inhalation concentration and ventilator ventilation time during surgery. This results in a reduced PaO2 in arterial blood, thereby accelerating the rapid appearance of the ISP. Thus, the investigators conducted a prospective, randomized, controlled trial to ascertain whether the oxygen partial pressure control method affects the occurrence time of the ISP and PaO2 during one-lung ventilation, in comparison to the modified inflation-deflation method. Furthermore, the objective was to confirm the safety and efficacy of Partial pressure of Oxygen Control method.

CONDITIONS

Official Title

Partial Pressure of Oxygen Control Method in Identification of Intersegmental Plane

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Between the ages of 18 and 75
  • Any gender
  • Eastern Cooperative Oncology Group (ECOG) Performance Status score of 0-1
  • Thin slice CT showing maximum tumor diameter of 2.0 cm or less and Consolidation Tumor Ratio (CTR) between 0 and less than 1.0
  • Willing and able to voluntarily sign informed consent and comply with study visit plan and protocols
Not Eligible

You will not qualify if you...

  • History of lung surgery
  • Diagnosis of interstitial pneumonia, pulmonary alveoli, pulmonary fibrosis, or severe emphysema
  • Undergoing chest surgery for other reasons or if surgical plan changes during operation
  • Unable or unwilling to understand, cooperate, or sign informed consent regarding the study protocol

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Trial Site Locations

Total: 1 location

1

The Second Affiliated Hospital of the Air Force Medical University of PLA

Xi'an, Shaanxi, China, 710000

Actively Recruiting

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Research Team

X

Xiaolong Yan, MD

CONTACT

M

Mingliang Xing

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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