Clinical Trials in Taiwan / NCT07436598
Recruiting Observational

3D Virtual Resection for Predicting Lung Function in VATS

NCT07436598 · tracked via the Priya Life Science Taiwan tracker
Phase
Observational
Started
2026-04-07
Last updated
2026-05-13

Condition(s) studied

Non-small Cell Lung CancerLung CancerLung Neoplasms

Study summary

This study aims to validate a novel preoperative assessment strategy using three-dimensional (3-D) computed tomography (CT) reconstruction and virtual resection simulation. The goal is to accurately predict postoperative pulmonary function in patients with non-small cell lung cancer (NSCLC) undergoing Video-Assisted Thoracoscopic Surgery (VATS) anatomical resection.

Accurate prediction of postoperative lung function is crucial for patient safety. Traditional methods, such as segment counting, often lack precision because they assume all lung segments contribute equally to function, ignoring variations caused by tumors or emphysema. This study utilizes 3-D "virtual resection" to quantify the "Planned Resected Ventilated Lung Volume Fraction" (pRVLVF) before surgery.

The study will recruit 60 participants divided into two groups: those undergoing lobectomy (n=30) and those undergoing segmentectomy (n=30). Participants will undergo standard thin-slice CT scans and pulmonary function tests (PFT) before surgery. Postoperatively, lung function and recovery will be tracked at 3, 6, and 12 months to develop a dynamic prediction model and evaluate the compensatory capacity of the residual lung.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Patients scheduled for video-assisted thoracoscopic (VATS) lobectomy or segmentectomy at National Taiwan University Hospital or NTU Cancer Center. * Age between 18 and 80 years. * Patients who have signed the informed consent form agreeing to provide imaging data for 3D modeling. Exclusion Criteria: * Age younger than 18 or older than 80 years. * Patients not scheduled for VATS lobectomy or segmentectomy. * Patients diagnosed with Chronic Obstructive Pulmonary Disease (COPD). * Patients unable or unwilling to sign the informed consent form. * Vulnerable populations.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
National Taiwan University Cancer Center Taipei Taiwan Recruiting

More National Taiwan University Hospital trials in Taiwan

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07436598 on ClinicalTrials.gov ↗ ← All trials in Taiwan