New surgical stapler put to the test in 244 patients
NCT ID NCT05519215
First seen Nov 01, 2025 · Last updated May 25, 2026 · Updated 40 times
Summary
This study tested a new powered stapler (ECHELON 3000) in 244 people having either stomach reduction surgery or lung removal surgery. The main goal was to see if the device caused serious side effects like infection, bleeding, or air leaks. The study is complete and helps doctors understand how safe and effective this tool is.
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This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Locations
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Ascension Providence Hospital
Southfield, Michigan, 48075, United States
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Bariatric Medical Institute of Texas
San Antonio, Texas, 78258, United States
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Cedars-Sinai Medical Center
Los Angeles, California, 90048, United States
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Emory Cardiothoracic Surgery
Atlanta, Georgia, 30322, United States
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George Washington University Hospital
Washington D.C., District of Columbia, 20037, United States
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Henry Ford Health Center
Detroit, Michigan, 48202, United States
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Long Island Jewish Medical Center
New Hyde Park, New York, 11040, United States
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Mayo Clinic
Rochester, Minnesota, 55905, United States
Conditions
Explore the condition pages connected to this study.