Skip to main content
Clinical Trials/NCT04004494
NCT04004494CompletedNot Applicable

Three-dimensional Computed Tomography Reconstruction for Operative Planning in VATS Segmentectomy

Ruijin Hospital3 sites in 1 country191 target enrollmentStarted: July 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
191
Locations
3
Primary Endpoint
operative time

Study Overview

Brief Summary

Anatomical variations of pulmonary vessel may cause serious problems during pulmonary segmentectomy. Three-dimensional (3D)computed tomography (CT) presents 3D images of pulmonary vessels and the tracheobronchial tree and may help operative planning. Retrospective studies have identified the importance of 3-dimensional CT in the field of pulmonary segmentectomy. And the aim of this study is to compare the usefulness of 3-dimensional CT with standard chest CT in preoperative planning of video-assisted segmentectomy.

Detailed Description

Lung cancer has been the most serious malignancy around the world which has the highest morbidity and mortality amount all the malignant tumors. Due to the wide spread of lung cancer screening, more and more early stage lung cancer patients have been diagnosed. Video-assisted segmentectomy is a standard surgical procedure in treating early stage peripheral non-small cell lung cancer (NSCLC). However, anatomical variations of pulmonary vessel may cause serious problems, for example unexpected bleed during surgery. Three-dimensional computed tomography (CT), which is reconstructed based on the standard chest CT image, presents 3D images of pulmonary vessels and the tracheobronchial tree and therefore helps operative planning. There are several retrospective studies addressed the importance of 3-dimensional CT in the field of pulmonary segmentectomy. And the aim of this multicenter randomized controlled trial is to compare the usefulness of 3-dimensional CT and standard chest CT in preoperative planning of video-assisted segmentectomy.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • •Age older than 18 years;
  • •Pulmonary nodules or ground glass opacification (GGO) found in chest CT examination, and conform with indications for segmentectomy:
  • •Peripheral nodule 0.8-2 cm with at least one of the following:
  • •i. Histology of adenocarcinoma in situ; ii. Nodule has ≥50% ground-glass appearance on CT; iii. Radiologic surveillance confirms a long doubling time (≥400 days). Segmentectomy should achieve parenchymal resection margins ≥2 cm or ≥ the size of the nodule.
  • •Adequate cardiac function, respiratory function, liver function and renal function for anesthesia and VATS segmentectomy.
  • •American Society of Anesthesiologists (ASA) score: Grade I-III.
  • •Patients who can coordinate the treatment and research and sign the informed consent.

Exclusion Criteria

  • •Patients with a significant medical condition which is thought unlikely to tolerate the surgery. For example, cardiac disease, significant liver and renal function disorder.
  • •Patients with psychiatric disease who are expected lack of compliance with the protocol.
  • •Patients have history of chest trauma or surgery on ipsilateral chest which may cause pleural adhesion.

Arms & Interventions

Chest computed tomography

No Intervention

Chest contrast-enhanced computed tomography will be performed preoperatively. Video-assisted segmentectomy will be performed based on the image of preoperative chest CT

3D Reconstruction

Experimental

Chest contrast-enhanced computed tomography will be performed preoperatively, and 3-dimensional reconstruction will be formed based on the data of chest CT. Video-assisted segmentectomy will be performed guided by the image of 3-dimensional CT. IPS-lung software (Shenzhen Yorktal Digital Medical Imaging Technology Company, Shenzhen, China) will be used preoperatively to construct a 3D-image to ascertain the position and structure of targeted segmental blood vessels and bronchi.

Intervention: 3D reconstruction (Other)

Outcomes

Primary Outcomes

operative time

Time Frame: During surgery

the time of operation

Secondary Outcomes

  • Disease-free survival (DFS)(up to 60 months)
  • Duration of chest tube placement(Up to 4 weeks)
  • Postoperative hospital stay(Up to 24 weeks)
  • blood loss(During surgery)
  • Incidence of postoperative complications(Postoperative in-hospital stay up to 30 days)
  • conversion rate(During surgery)
  • 30-day mortality(Postoperative in-hospital stay up to 30 days)
  • operative accident event(During surgery)
  • dissection of lymph nodes(2 weeks after surgery)
  • Preoperative lung function(Baseline)
  • Postoperative lung function(at the 3rd month after surgery)
  • Overall survival (OS)(up to 60 months)
  • Incidence of change of surgical plan(During surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hecheng Li M.D., Ph.D

Professor

Ruijin Hospital

Study Sites (3)

Loading locations...

Similar Trials