Uro-NIRS Clinical Study

NACompletedINTERVENTIONAL
Enrollment

42

Participants

Timeline

Start Date

April 30, 2008

Primary Completion Date

May 31, 2010

Study Completion Date

May 31, 2010

Conditions
Lower Urinary Tract SymptomsOveractive Bladder
Interventions
DEVICE

Fully integrated Uro-NIRS:UDS

As part of standard care subjects will be undergoing a standard bladder pressure diagnostic procedure. This standard procedure will involve the insertion of a catheter (a plastic tube) into the urethra and the measurement of pressure within the bladder. For subjects taking part in this study, the health of the bladder will measured by using light instead of pressure. A patch, the size of cell phone or deck of playing cards, will be taped to the skin in the middle of the abdomen, above the bladder. Using laser light that is 300 billion times weaker than the light from a regular household 100-Watt light bulb, the Laborie and Urodynamix device will take measurements through the skin without inserting anything into the body.

Trial Locations (1)

10065

New York-Presbyterian Hospital Weill Cornell Medical Center, New York

Sponsors
All Listed Sponsors
collaborator

Urodynamix Technologies

INDUSTRY

collaborator

Laborie Medical Technologies Inc.

INDUSTRY

lead

Weill Medical College of Cornell University

OTHER

NCT00706407 - Uro-NIRS Clinical Study | Biotech Hunter | Biotech Hunter