Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT07065604

Tubeless VATS for Mediastinal Neoplasm

Led by Shuben Li · Updated on 2025-07-15

132

Participants Needed

1

Research Sites

179 weeks

Total Duration

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Sponsors

S

Shuben Li

Lead Sponsor

T

The First Affiliated Hospital of Guangzhou Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

In recent year, non-intubated anesthesia had emerged as an available and promising alternative for thoracic procedure. However, its safety and feasibility in video-assisted thoracoscopic surgery (VATS) for mediastinal neoplasm remain controversial. This randomized controlled trial is designed to evaluate the impact of the non-intubated approach on surgical and perioperative outcomes in patients undergoing mediastinal neoplasm resection.

CONDITIONS

Official Title

Tubeless VATS for Mediastinal Neoplasm

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Mediastinal neoplasm diagnosed by chest enhanced CT
  • Age between 18 and 80 years old
  • Tumor diameter less than 6 cm
  • ASA grade I to III
  • Ability to understand the research and provide informed consent
Not Eligible

You will not qualify if you...

  • Tumor invading adjacent organs or evidence of pleural/pericardial spread or metastases
  • History of congestive heart failure, poorly controlled angina, recent myocardial infarction, uncontrolled hypertension, significant valvular heart disease, or unmanaged high-risk arrhythmias
  • Presence of other active malignancies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

the First Affiliated Hospital of Guangzhou Medical University

Guangzhou, Guangdong, China, 510120

Actively Recruiting

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Research Team

S

Shuben Li, Deputy Director

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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