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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03106103
Other study ID # EYH-2014
Secondary ID
Status Completed
Phase N/A
First received June 10, 2014
Last updated April 4, 2017
Start date February 2009
Est. completion date December 2014

Study information

Verified date April 2017
Source Federal University of São Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Urodynamic Study (UDS) represents a series of agreed-upon clinical tests and is used to evaluate the functional status of the lower urinary tract, providing a pathophysiological basis for urinary symptoms. Urodynamic Study involves catheterization of the lower urinary tract. The prevalence of urinary tract infection after UDS ranges from 1,5% to 30 %.

Studies of prophylactic antibiotics for UDSs have offered data of contradictory and limited predictive values. Some investigators concluded that prophylactic antibiotics were valuable and others have not.

The objective of this study is to evaluate the efficacy of antibiotic prophylaxis before UDS in women, using different antibiotic regimens.


Description:

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Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Federal University of São Paulo

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of symptomatic and asymptomatic bacteriuria after urodynamic study in women with urinary incontinence 24 months
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