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NCT01282840 Clinical Trial

Bladder Wall Blood Perfusion Pattern and Sexual Dysfunction in Female Patients With Lower Urinary Tract Symptoms, and the Association of That Perfusion Pattern and Therapeutic Efficacy of Antimuscarincs for Female Overactive Bladder Syndrome.

Lower Urinary Tract Symptoms Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01282840
Other study ID # 099049-F
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 20, 2010
Est. completion date December 26, 2018

Study information
Verified date November 2018
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Overactive bladder syndrome (OAB) affects around 17 % of female population. However, the etiology of OAB is complicated and unclear in many aspects. Bladder wall thickness had been reported to be strongly associated with OAB, but its use as a screening tool remains controversial. Besides, few studies reported patterns of sexual dysfunction in female patients with lower urinary tract symptoms (LUTS). Therefore the aims of our study were to analyze the bladder wall blood perfusion pattern in female LUTS patients, the association of between the bladder wall blood perfusion pattern and the efficacy of anti-muscarinic treatment for female OAB, and the patterns of sexual dysfunction in the female LUTS patients.

Recruitment information / eligibility
Status Completed
Enrollment 676
Est. completion date December 26, 2018
Est. primary completion date November 5, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 99 Years
Eligibility Inclusion Criteria:

- all cases are female patients with lower urinary tract symptoms

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Tolterodine SR
Tolterodine SR 4 mg qd

Locations
Country Name City State
Taiwan Far Eastern Memorial Hospital New Taipei Banqiao

Sponsors (2)
Lead Sponsor Collaborator
Far Eastern Memorial Hospital National Science Council, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Blood flow pattern after antimuscarinics 12 weeks
Secondary Blood flow patterns between different LUTS subgroups 1 day
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