MedTrace Logo

Needlescopic-assisted Uniportal vs Uniportal VATS

NCT03439696 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2021-02-25

No results posted yet for this study

Summary

The investigators' study aims is to evaluate the safety and efficacy of uniportal VATS under assistance of needlescopic instruments through additional 2-3 mm ports compared to conventional uniportal VATS in patients with lung lesions.

Conditions

  • Lung Cancer
  • Lung Cancer Metastatic
  • Bullous Disease Lung
  • Nodule Solitary Pulmonary
  • Mediastinal Tumor

Interventions

PROCEDURE

Thoracoscopic surgery

Video-assisted thoracoscopic surgery for pulmonary or mediastinal lesions.

Sponsors & Collaborators

  • IRB of NTUH Hsin-Chu Branch

    lead OTHER

Principal Investigators

  • Chiu-kuei Nien · National Taiwan University Hospital Hsinchu Branch

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-02-22
Primary Completion
2018-12-12
Completion
2019-04-30

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03439696 on ClinicalTrials.gov