Bladder Cancer Clinical Trial
A Prospective Randomized Controlled Clinical Trial of Standard Versus Goal-Directed Perioperative Fluid Management (GDT) for Patients Undergoing Radical Cystectomy
Summary
The purpose of this study is to help us learn what is the best amount of fluid to give to patients during bladder surgery in order to avoid delayed bowel function after surgery, which could prolong hospital stay.
Eligibility Criteria
Inclusion Criteria:
Adults (21 years old or greater) who are able to provide informed consent
Patients who undergo an open, elective radical cystectomy
Exclusion Criteria:
Patients with active atrial fibrillation or flutter, since the algorithm is not accurate in case of cardiac arrhythmia
Female patients who are pregnant (female patients of child-bearing potential must have a negative serum pregnancy test ≤ 14 days prior to surgery or 15 to 30 days prior to surgery with a negative urine pregnancy test the morning of surgery)
Presence of ascites, because increased abdominal pressure interferes with EV1000 reading accuracy
BMI > 45 or <17, because increased abdominal pressure interferes with EV1000 reading accuracy
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There are 5 Locations for this study
Basking Ridge New Jersey, 07920, United States
Middletown New Jersey, 07748, United States
Commack New York, 11725, United States
Harrison New York, 10604, United States
New York New York, 10021, United States
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