NIPH Clinical Trials Search

Basic Information

Recruitment status
Health condition(s) or Problem(s) studied	Overactive bladder
Date of first enrollment	05/09/2005
Target sample size
Countries of recruitment
Study type	Interventional
Intervention(s)	investigational material(s) Generic name etc : CS-801 INN of investigational material : Therapeutic category code : 259 Other agents for uro-genital and anal organ Dosage and Administration for Investigational material : Transdermal

Outcome(s)

Primary Outcome	Efficacy and safety
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum	>= 20age old
Age maximum	Not applicable
Gender
Include criteria	Inclusion criteria: -Patient, age 20 years or older -Patients with urinary frequency and urge urinary incontinence Exclusion criteria: -Patients who have diseases such as dysuria or urinary retention -Patients who have difficulty to void for myself -Patients with other diseases which may have been related to the state of urination. (ex urinary tract infection) -Patients with polyuria -Patients with diseases for which treatment with anticholinergic agents is contraindicated -Patients in whom precautions are required for the use of anticholinergic agents -Patients who have difficulty to use transdermal medications
Exclude criteria