Prospective Randomized Trial of the Effectiveness of Managing Postoperative Air Leak between Electronic Versus Traditional Chest Drainage System in Pulmonary Resectio
Not Applicable
- Conditions
- ung cancer
- Registration Number
- JPRN-UMIN000016715
- Lead Sponsor
- General Thoracic Surgery, Juntendo University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
Not provided
Exclusion Criteria
1)Has previously undergone ipsilateral lung surgery 2)Has an active lung infection (bacterial infection or fungal infection) 3)Undergoing continuing systemic administration (oral or intravenous) of steroids 4)Complicated by uncontrolled diabetes mellitus (Uncontrolled: urinary glucose of 10 g or more per day or fasting blood glucose of 150 mg/dL or more even under insulin treatment) 5)Requiring anticoagulant therapy (continuous intravenous drip of heparin) in the perioperative period 6)Patient participation in the study is judged difficult due to complications related to a psychiatric disorder or psychological symptoms 7)Judged unsuitable for study participation by the investigator for any other reason
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of drain placement (days)
- Secondary Outcome Measures
Name Time Method Percent occurrence of intraoperative air leak (at the time of the first postoperative leak test), frequency of intraoperative sealant use and its type, percent occurrence of postoperative air leak (at the time of entering postoperative recovery room or ICU), duration of postoperative air leak (days), frequency of postoperative pleurodesis, days of hospitalization (days), and percent occurrence of postoperative adverse events