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Brief Title: Efficacy and Safety of Aprotinin on Transfusion Requirements in Patients Undergoing Radical or Total Cystectomy
Official Title: A Multi-center, Randomized, Double Blind, Placebo Controlled Study to Investigate the Efficacy and Safety of Aprotinin on Transfusion Requirements in Patients With Bladder Cancer Undergoing Radical or Total Cystectomy.
Study ID: NCT00306150
Brief Summary: The purpose of this study is to assess if aprotinin (BAYA0128), given intravenously during your surgery, is safe and can help reduce the need for a blood transfusion during bladder surgery.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
, Los Angeles, California, United States
, Denver, Colorado, United States
, Miami, Florida, United States
, Chicago, Illinois, United States
, Chicago, Illinois, United States
, Portland, Maine, United States
, Baltimore, Maryland, United States
, Ann Arbor, Michigan, United States
, Rochester, Minnesota, United States
, Chapel Hill, North Carolina, United States
, Cleveland, Ohio, United States
, Columbus, Ohio, United States
, Oklahoma City, Oklahoma, United States
, Philadelphia, Pennsylvania, United States
, Pittsburgh, Pennsylvania, United States
, Nashville, Tennessee, United States
, Houston, Texas, United States
, Burlington, Vermont, United States
, Gent, , Belgium
, Leuven, , Belgium
, Nantes Cedex, , France
, Nice, , France
, Tübingen, Baden-Württemberg, Germany
, München, Bayern, Germany
, Regensburg, Bayern, Germany
, Fulda, Hessen, Germany
, Mainz, Rheinland-Pfalz, Germany
, Homburg, Saarland, Germany
, Dresden, Sachsen, Germany
, Maastricht, , Netherlands
, Nijmegen, , Netherlands
, Linköping, , Sweden
, Lund, , Sweden
, Stockholm, , Sweden
, Uppsala, , Sweden
, Cambridge, Cambridgeshire, United Kingdom
, Newcastle Upon Tyne, Tyne and Wear, United Kingdom
Name: Bayer Study Director
Affiliation: Bayer
Role: STUDY_DIRECTOR