Actively Recruiting
Tubeless Anesthesia in Preventing Lung Complications in Patients Undergoing Surgery for Early-Stage Lung Cancer
Led by Fujian Medical University Union Hospital · Updated on 2025-06-17
224
Participants Needed
1
Research Sites
131 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study focuses on evaluating the effectiveness and safety of tubeless anesthesia in single-port thoracoscopic surgery for early-stage lung cancer patients. Traditional anesthesia methods risk postoperative complications like lung injury and respiratory issues. Tubeless anesthesia preserves spontaneous breathing without tracheal intubation, potentially reducing these complications and enhancing recovery. The study aims to compare this technique with traditional methods, assessing its impact on contralateral lung complications, perioperative hemodynamics, complication rates, and recovery speed.
CONDITIONS
Official Title
Tubeless Anesthesia in Preventing Lung Complications in Patients Undergoing Surgery for Early-Stage Lung Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 to 70 years
- ECOG performance status score 0-1
- Good cardiac and pulmonary function
- Single or multiple peripheral lung nodules planned for single-port thoracoscopic surgery, with or without mediastinal lymph node dissection or sampling
- Able to comply with the study visit schedule and other protocol requirements
- Signed informed consent and voluntary participation in the study
You will not qualify if you...
- Obesity with body mass index over 30
- Difficult intubation or expected complex airway management
- Chronic obstructive pulmonary disease with large airway secretions
- Neurological dysfunction or inability to cooperate while awake
- Expected extensive pleural adhesions or previous lung resection
- Severe hypoxia or hypercapnia in elderly or frail patients
- Previous induction chemotherapy or chemoradiotherapy
- Need during surgery to isolate the lung to prevent contamination
- Expected large surgical wounds and lengthy procedures
- Cardiac or pulmonary function or overall health unsuitable for the procedure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Fujian Medical University Union Hospital
Fuzhou, Fujian, China, 350001
Actively Recruiting
Research Team
S
Shishi Huang
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here