283
Participants
Start Date
February 29, 2008
Primary Completion Date
September 30, 2010
Study Completion Date
September 30, 2010
Hexaminolevulinate (Hexvix)
Each patient enrolled into the study will be infused with 50 mL of a 2 mg/mL Hexvix solution in the bladder using a catheter. Subsequently, after fluid retention by the patient in the bladder for one hour, the bladder will be emptied.
GE Healthcare, Madrid
Lead Sponsor
GE Healthcare
INDUSTRY