Due to the lapse in government funding, the information on this web site may not be up to date, transactions submitted via the web site may not be processed,
and the agency may not be able to respond to inquiries until appropriations are enacted. Updates regarding government
operating status and resumption of normal operations can be found at opm.gov.
Controlled Study of ONO-8025 (KRP-197) in Patients With Overactive Bladder in Japan
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government.
Read our disclaimer for details.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study:
20 Years and older (Adult, Senior)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Patients who are 20 years old or over with overactive bladder
Total number of urinary incontinence episodes per week is 5 or over
Mean number of micturition per day is 8 or over
Mean number of urinary urgency episodes per day is 1 or over
Other inclusion criteria as specified in the study protocol
Patients with genuine stress incontinence
Patients suffering from complications such as bladder tumor, bladder stone and urinary tract infection
Patients who have undergone surgical operation of urinary and/or genital organs within 6 months prior to the study
Patients suffering from complications for which anticholinergics are contraindicated
Other exclusion criteria as specified in the study protocol