Actively Recruiting
Effects of Different Occlusion Angles of Disposable Tracheal Blocker on Right One-lung Ventilation
Led by China Medical University, China · Updated on 2024-09-19
96
Participants Needed
3
Research Sites
64 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This trial is a practical, multicenter, prospective, parallel grouping, randomized controlled,two-arm study. This study will be conducted in three centers including the First Hospital of China Medical University, Seoul National University Hospital and the University Clinical Center of Serbia. The investigators aim to investigate the effect of different occlusion angles of disposable tracheal blocker on right one-lung ventilation
CONDITIONS
Official Title
Effects of Different Occlusion Angles of Disposable Tracheal Blocker on Right One-lung Ventilation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age ranged from 18 to 65 years old
- American Society of Anesthesiologists (ASA) grade I-III
- No history of drug allergy or abnormal anesthesia
- Patients undergoing right thoracoscopic surgery
- The preoperative oxygen saturation was not less than 94%
You will not qualify if you...
- History of acute lung injury or ARDS within 3 months
- Cardiac function class IV (New York Heart Association classification)
- Chronic renal failure (renal cell filtration rate <30ml min-11.73m-2), severe liver disease
- Blurred consciousness and cognitive dysfunction
- Severe coagulation dysfunction
- Without preoperative oxygen inhalation, blood oxygen <94%, severe pulmonary dysfunction
- Patients with endotracheal tube admitted to ICU after operation
- Body mass index (BMI) >30
- Patients who had had lung surgery
- Inability to complete the study
AI-Screening
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Trial Site Locations
Total: 3 locations
1
Wenfei Tan
Shenyang, China
Actively Recruiting
2
the University Clinical Center of Serbia
Belgrade, Serbia
Not Yet Recruiting
3
Konkuk University School of Medicine
Seoul, South Korea
Not Yet Recruiting
Research Team
W
Wenfei Tan
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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