70
Participants
Start Date
July 31, 2006
Primary Completion Date
May 31, 2008
Study Completion Date
May 31, 2008
Cyberwand
FDA approved - dual probe intracorporeal lithotrite
single probe ultrasonic
FDA-approved - single probe ultrasonic
Duke University, Durham
Methodist Hospital, Indianapolis
University of Wisconsin, Madison
Northwestern University Dept. of Urology, Chicago
John's Hopkins University, Baltimore
Vancouver Hospital, Vancouver
University of Western Ontario - St. Joseph's Hospital, London
Indiana Kidney Stone Institute
OTHER