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Spots Global Cancer Trial Database for Efficacy and Safety of Aprotinin on Transfusion Requirements in Patients Undergoing Radical or Total Cystectomy

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We do not endorse or review these studies in any way.

Trial Identification

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

Study Description

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:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

, 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

Contact Details

Name: Bayer Study Director

Affiliation: Bayer

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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