Tubeless VATS for Mediastinal Neoplasm
Launched by SHUBEN LI · Jul 4, 2025
Trial Information
Current as of August 22, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new way to perform surgery to remove tumors located in the middle part of the chest, called the mediastinum. Usually, such surgeries use a breathing tube and general anesthesia, but this trial is testing a technique called “tubeless” video-assisted thoracoscopic surgery (VATS), which uses a less invasive form of anesthesia without placing a breathing tube. The goal is to see if this method is safe and if it helps patients recover better after surgery.
Adults between 18 and 80 years old who have a tumor smaller than 6 centimeters in the mediastinum, confirmed by a CT scan, may be eligible to join. To participate, patients need to be in reasonably good health (based on a standard health assessment) and able to understand the study and give consent. People with tumors that have spread to nearby organs or with serious heart problems or other active cancers cannot join. If you take part, you can expect to have surgery using this less invasive anesthesia approach, and the doctors will carefully monitor how well it works and how it affects recovery. This study is currently recruiting patients and aims to find out if this tubeless method is a safe and effective option for mediastinal tumor surgery.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Mediastinal neoplasm was diagnosed by chest enhanced CT
- • 2. The patients with age ≥ 18 and ≤ 80 years old
- • 3. The patients whose tumor diameter was \<6 cm
- • 4. ASA grade: I-III
- • 5. The patients should understand the research and sign the informed consent
- Exclusion Criteria:
- • 1. Imaging examinations revealed that the tumor had invaded adjacent organs, with evidence of pleural or pericardial dissemination, as well as lymphatic and/or hematogenous metastases
- • 2. Patients with a confirmed history of congestive heart failure, poorly controlled angina despite medical therapy, electrocardiogram-confirmed myocardial infarction with transmural involvement, uncontrolled hypertension, clinically significant valvular heart disease, or high-risk arrhythmias not adequately managed
- • 3. Patients with concurrent active malignancies
About Shuben Li
Shuben Li is a clinical trial sponsor committed to advancing medical research and innovation. With a focus on developing effective and safe therapeutic interventions, Shuben Li supports rigorous clinical studies aimed at improving patient outcomes across various medical disciplines. Through collaboration with research institutions and adherence to regulatory standards, the sponsor strives to contribute valuable scientific knowledge to the healthcare community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Guangzhou, Guangdong, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported