Urinary Urgency Outcomes Following Propiverine Treatment for an Overactive Bladder
Primary Purpose
Overactive Bladder
Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Propiverine hydrochloride
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Overactive Bladder focused on measuring Overactive bladder, Propiverin
Eligibility Criteria
Inclusion Criteria:
- age ≥ 18 years
- Overactive bladder for at least 3 months
3 day- voiding diary
- average urinary frequency ≥ 10 voids/24hrs
- urgency ≥ 2 episodes/24hrs
- "moderate to severe" in the Indevus Urgency Severity Scale (IUSS)
Exclusion Criteria:
- clinically significant stress urinary incontinence
- polyuria of more than 3000 ml/24 hrs
- severe hepatic or renal diseases
- contraindications to the use of antimuscarinic drugs
- genitourinary conditions that could cause OAB symptoms such as urinary tract infection, genitourinary malignancy or interstitial cystitis
- uninvestigated hematuria
- clinically significant bladder outlet obstruction
- clinically significant pelvic organ prolapse
- being on a bladder-training program or having been on electrostimulation therapy two weeks before randomization or intention to start
- unstable dosages of drugs with anticholinergic side effects
- any other investigational drug taken up to 2 months prior to randomization
- pregnancy or breastfeeding
Sites / Locations
- Samsung Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
1
2
Arm Description
Outcomes
Primary Outcome Measures
Percent change in mean number of urgency episode
Secondary Outcome Measures
Change in the patients' perception of urgency
Change in urgency severity/voids
Change in sum of urgency severity/24 hours
Changes in voiding frequency/24hrs, daytime and nocturnal voiding frequency/24 hours
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00903045
Brief Title
Urinary Urgency Outcomes Following Propiverine Treatment for an Overactive Bladder
Official Title
Urinary Urgency Outcomes Following Propiverine Treatment for an Overactive Bladder: PRopiverine Study on Overactive Bladder Including Urgency Data (PROUD)
Study Type
Interventional
2. Study Status
Record Verification Date
May 2009
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
August 2006 (Actual)
Study Completion Date
August 2006 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Samsung Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Overactive bladder (OAB) is defined as "urgency, with or without urge incontinence, usually with frequency and nocturia" in the absence of local pathological or endocrine factors. Urgency is defined as "the complaint of a sudden compelling desire to pass urine that is difficult to defer" and an abnormal sensation that is distinctly different from the normal physiologic feeling of 'urge to void' that occurs during typical bladder-filling cycles.
Because up to 50% of patients with OAB experience urgency without incontinence, and because urgency is the most bothersome symptom that drives behavioral adaptations such as frequent voiding because of the very fear of urgency, this is the cornerstone symptom of OAB that indicates the diagnosis of OAB.
Even though any effective treatment for OAB must reduce the patient's sense of urgency, its subjective nature makes it difficult to measure. Therefore, the clinical efficacy of OAB treatment was traditionally measured in terms of objective surrogate parameters instead of urgency itself: for example, change in urinary frequency, incontinent episodes, number of pads and urodynamically proven detrusor overactivity, which could be measured easily and quantifiably.
Recently, several methods that measure urgency have been developed and used in clinical practice. However, the analysis questioned the clinical significance of the results; a possible reason for this being the lack of data based on urinary urgency and the use of sensitive patient-driven criteria.
Propiverine hydrochloride (1-methyl-4-piperidyl diphenylpropoxyacetate hydrochloride) is a drug with combined antimuscarinic and calcium antagonistic actions. Previous trials on the clinical efficacy and safety of propiverine for treating patients with OAB have reported improvements in urinary frequency and incontinence, but not in urgency.
The aim of this study was to explore the efficacy of a daily regimen of propiverine at 20 mg (immediate release formulation) in improving urgency from baseline to 12 weeks of treatment in patients with OAB.
Detailed Description
12-week multi-center, prospective, parallel, double-blind, placebo-controlled trial
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overactive Bladder
Keywords
Overactive bladder, Propiverin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
264 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Propiverine hydrochloride
Other Intervention Name(s)
BUP-4
Intervention Description
Propiverine hydrochloride 20mg twice a day
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Identical placebo twice a day
Primary Outcome Measure Information:
Title
Percent change in mean number of urgency episode
Time Frame
12 weeks of treatment
Secondary Outcome Measure Information:
Title
Change in the patients' perception of urgency
Time Frame
12 weeks of treatment
Title
Change in urgency severity/voids
Time Frame
12 weeks of treatment
Title
Change in sum of urgency severity/24 hours
Time Frame
12 weeks of treatment
Title
Changes in voiding frequency/24hrs, daytime and nocturnal voiding frequency/24 hours
Time Frame
12 weeks of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age ≥ 18 years
Overactive bladder for at least 3 months
3 day- voiding diary
average urinary frequency ≥ 10 voids/24hrs
urgency ≥ 2 episodes/24hrs
"moderate to severe" in the Indevus Urgency Severity Scale (IUSS)
Exclusion Criteria:
clinically significant stress urinary incontinence
polyuria of more than 3000 ml/24 hrs
severe hepatic or renal diseases
contraindications to the use of antimuscarinic drugs
genitourinary conditions that could cause OAB symptoms such as urinary tract infection, genitourinary malignancy or interstitial cystitis
uninvestigated hematuria
clinically significant bladder outlet obstruction
clinically significant pelvic organ prolapse
being on a bladder-training program or having been on electrostimulation therapy two weeks before randomization or intention to start
unstable dosages of drugs with anticholinergic side effects
any other investigational drug taken up to 2 months prior to randomization
pregnancy or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kyu-Sung Lee, Ph.D
Organizational Affiliation
Samsung Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
Country
Korea, Republic of
12. IPD Sharing Statement
Citations:
PubMed Identifier
19912183
Citation
Lee KS, Lee HW, Choo MS, Paick JS, Lee JG, Seo JT, Lee JZ, Lee YS, Yoon H, Park CH, Na YG, Jeong YB, Lee JB, Park WH. Urinary urgency outcomes after propiverine treatment for an overactive bladder: the 'Propiverine study on overactive bladder including urgency data'. BJU Int. 2010 Jun;105(11):1565-70. doi: 10.1111/j.1464-410X.2009.09050.x. Epub 2009 Nov 12.
Results Reference
derived
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Urinary Urgency Outcomes Following Propiverine Treatment for an Overactive Bladder
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