Evaluation of the effect onset with Propiverine hydrochloride(BUP-4) in Female Patients diagnosed as overactive bladder.
- Conditions
- overactive bladder
- Registration Number
- JPRN-UMIN000012512
- Lead Sponsor
- Saitama Continence Conference
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 30
Not provided
1) Patients with bladder stone, urethral calculus, interstitial cystitis 2) Patients with endometriosis required for surgery and pelvic organ prolapse 3) Patients with history of treatment OAB within 2 months 4) Patients with treatment for cancer 5) Patients with lower urinary tract symptom 6) Patients with symptomatic urinary tract infection 7) Patients with polyuria (>=3000mL /day) 8) Other severe complications, such as uncontrolled diabetes mellitus, uncontrolled hypertension) 9) Patients with angle-closure glaucoma 10) Patients with severe heart dysfunction, renal dysfunction, liver dysfunction 11) Women who are capable of pregnancy, intend to get pregnant 12) Pregnant or lactating women 13) Judged ineligible based on physicians' decision
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method change of frequency of urination in 24 hours
- Secondary Outcome Measures
Name Time Method change of urinary urgency in 24 hours, change of urinary incontinence in 24 hours, change of OABSS score, change of KHQ score, Residual urine volume, adverse event