Study of Postoperative Chest Tube Management
Completed · Phase 4
Conditions studied: Lung Resection
In brief
A 2 x 2 randomized study testing active versus passive drainage and regulated versus unregulated pleural pressure in patients undergoing anatomic lung resection
Key facts
- Study ID
- NCT02282462
- Run by
- Yale University
- People needed
- 600
- Starts
- 2014-12-01
- Expected to finish
- 2017-12-18
- Last updated by the study team
- 2020-06-26
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Able and willing to read, understand, and provide written consent
- Age 18-90
- Undergoing a segmentectomy, lobectomy, or bilobectomy (including sleeve resection). Both open and minimally invasive (thoracoscopic or robotic) resections are acceptable
You may not qualify if…
- Patients unstable enough to require ICU care for hemodynamic or respiratory problems during the first 7 days postoperatively. Patients admitted to the ICU for other reasons (e.g. bed availability, institutional norm, routine monitoring etc.) should NOT be excluded
- Patients undergoing non-anatomic lung resection only (i.e. wedge resection)
- Patients undergoing anatomic lung resection for bullous disease, lung abscess or bronchiectasis.
- Patients undergoing pneumonectomy or completion pneumonectomy
Where it is running
- Yale University — New Haven, Connecticut, United States
- WellStar Health System - Kennestone — Marietta, Georgia, United States
- Beth Israel Deaconess/ Harvard — Boston, Massachusetts, United States
- Valley Health System — Paramus, New Jersey, United States
- St. Luke's Hospital — Bethlehem, Pennsylvania, United States
Full record on ClinicalTrials.gov
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