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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01876186
Other study ID # 201212143RINB
Secondary ID
Status Recruiting
Phase Phase 4
First received June 10, 2013
Last updated July 5, 2015
Start date May 2013
Est. completion date December 2015

Study information

Verified date July 2015
Source National Taiwan University Hospital
Contact Ho-Hsiung Lin, MD, PhD
Phone +886-2-23123456
Email hhlin@ntuh.gov.tw
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Interventional

Clinical Trial Summary

To investigate whether prolonged period of treatment (6 months) can have a better therapeutic outcome than conventional period (3 months) of antimuscarinics.


Description:

Overactive bladder syndrome (OAB), with or without urge incontinence, is characterized by urinary urgency, frequency and nocturia. Thus, patients with OAB could be considered to have a reduced quality of life. Patients with overactive bladder syndrome have a higher risk of falling and fracture due to nocturia. OAB affects around 17 % of female population. At present, muscarinic receptor antagonists are the first-line pharmacotherapeutic agents for OAB. However, discontinuation of the treatment often results in symptom relapse. Until now, optimal duration of the treatment and durability of the efficacy have not been determined. We plan to use urodynamic studies outcome to evaluate therapeutic effect, with the change of urinary nerve growth factor level. This study is a randomized prospective study, comparing female OAB patient after 3 months and 6 months of antimuscarinic treatment.

The purpose of this study is to investigate the difference of urodynamic effects, therapeutic effect and urinary urinary nerve growth factor level between OAB females after 3 months and 6 months antimuscarinic treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender Female
Age group 20 Years and older
Eligibility Inclusion Criteria:

- Women who have overactive bladder syndrome

Exclusion Criteria:

- Women who are less than 20 year-old

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
Solifenacin for 12 weeks
Solifenacin 5 mg one a day for 12 weeks
Solifenacin for 24 weeks
Solifenacin 5 mg once a day for 24 weeks

Locations

Country Name City State
Taiwan Department of Obstetrics & Gynecology, National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary The rate of normalized urodynamic findings The rate of normalized urodynamic finding after antimuscarinics 6 months No
Secondary The cure rate of overactive bladder The cure rate of overactive bladder after antimuscarinics 24 weeks No
Secondary The recurrence rate of overactive bladder The recurrence rate of overactive bladder after antimuscarinics 2.5 years No
Secondary The difference of urine nerve growth factor level The difference of urine nerve growth factor level after antimuscarinics 24 weeks No
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