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NCT07057531Completed

Tubeless VATS for Lung Cancer Surgery

A Prospective Randomized Controlled Study Evaluating Lung Injury, Long-term Clinical Outcomes, and Environmental Impact of Tubeless Versus Intubated Video-Assisted Thoracic Surgery for Lung Cancer Resection

Source: ClinicalTrials.gov · Last updated 19 Dec 2025

Brief summary (registry, in English)

This prospective cohort study evaluates lung injury, long-term clinical outcomes, and environmental impacts of tubeless video-assisted thoracic surgery (VATS) compared with conventional intubated VATS for lung cancer resection. The study aims to determine whether the tubeless approach reduces anesthetic exposure, minimizes lung injury, enhances patient recovery, and decreases carbon emissions, contributing toward sustainable surgical practices.

Status (registry)
Completed
Study type
Interventional
Enrollment
73 (actual)
First submitted
30 Jun 2025
Start date
25 Jul 2025
Primary completion date
5 Dec 2025
Lead sponsor
The First Affiliated Hospital of Guangzhou Medical University
Diseases
Lung cancer
NCT number
NCT07057531

What you commit to

  • Study type: Interventional
  • Participants enrolled: 73
  • From 25 Jul 2025 to the primary completion date, 5 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Emergency surgery due to acute respiratory or cardiovascular instability.
  • Inability to cooperate with the planned anesthetic and surgical protocols or postoperative follow-up procedures.

Other illness

  • History of severe cardiopulmonary disease or unstable medical conditions that contraindicate minimally invasive thoracic surgery.
  • Known allergy or contraindication to anesthetic agents or materials used in the study.

Other

  • Patients requiring bilateral pulmonary procedures or planned open thoracotomy.
  • Pregnancy or lactation at the time of enrollment.
  • Enrollment in another interventional clinical study within the past 30 days.

Who the study is looking for

  • Patients aged ≥18 years scheduled for elective video-assisted thoracic surgery (VATS) for confirmed or suspected lung cancer.
  • Clinical stage suitable for surgical resection (lobectomy, segmentectomy, or wedge resection).
  • American Society of Anesthesiologists (ASA) physical status classification ≤III.
  • Ability to understand and willingness to provide written informed consent.
  • Agreement to adhere to scheduled postoperative clinical follow-up assessments, including pulmonary function tests and survival status evaluations.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Affiliated Hospital of Guangzhou Medical University
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.