Status:

COMPLETED

Uro-NIRS Clinical Study

Lead Sponsor:

Weill Medical College of Cornell University

Collaborating Sponsors:

Urodynamix Technologies

Laborie Medical Technologies Inc.

Conditions:

Lower Urinary Tract Symptoms

Overactive Bladder

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this experiment is to confirm the results of previous testing of Urodynamix's Uro-NIRS device. Together Urodynamix and Laborie have created a device that includes standard Laborie medic...

Detailed Description

This is a study of the fully integrated Uro-NIRS:UDS device (Laborie Triton or Laborie Dorado and Urodynamix's Non-Invasive Urodynamics device - Uro-NIRS), to confirm the results using the fully integ...

Eligibility Criteria

Inclusion

  • Subjects must be 18 years of age or older.
  • Subjects are patients of one of the institutions and are currently scheduled for UDS
  • Male subjects must have LUTS
  • Female subjects must have OAB
  • Subjects must give their informed consent prior to enrollment.

Exclusion

  • The patient has an existing health condition which the investigators feel will not allow for safe or accurate measurements with the Uro-NIRS:UDS device.

Key Trial Info

Start Date :

April 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2010

Estimated Enrollment :

42 Patients enrolled

Trial Details

Trial ID

NCT00706407

Start Date

April 1 2008

End Date

May 1 2010

Last Update

March 13 2018

Active Locations (1)

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Page 1 of 1 (1 locations)

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New York-Presbyterian Hospital Weill Cornell Medical Center

New York, New York, United States, 10065

Uro-NIRS Clinical Study | DecenTrialz