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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00141128
Other study ID # A6061024
Secondary ID
Status Completed
Phase Phase 2
First received August 29, 2005
Last updated May 31, 2011
Start date December 2005
Est. completion date June 2006

Study information

Verified date May 2011
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Medicines Agency
Study type Interventional

Clinical Trial Summary

SS-RBX will be used to evaluate pharmacodynamic changes in urethral function using a novel methodology


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date June 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Female

- Stress urinary incontinence

Exclusion Criteria:

- Bladder outflow obstruction

- Neurological disease

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
SS-RBX


Locations

Country Name City State
Denmark Pfizer Investigational Site Glostrup

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary To assess the utility of urethral reflectometry in the detection of pharmacologically induced pressure changes in the female urethra.
Secondary To assess the effect of [S,S]-Reboxetine on urethral function in women with SUI.
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