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NCT00194532 · ClinicalTrials.gov registry record · NA
Cefpodoxime vs Ciprofloxacin for Acute Cystitis
A NA study of Urinary Tract Infection, sponsored by University of Washington.
- Completed
- Registry status
- NA
- Development phase
- 300
- Enrollment target
- 2
- Study locations
NCT00194532 is a NA study of Urinary Tract Infection that has completed, run by University of Washington. The registered enrollment target is 300 participants, below the 646-participant average among 11 other Urinary Tract Infection trials with a reported enrollment target (54% lower). The trial reports 2 study locations across 2 states.
The verdict
NCT00194532, a NA study of Urinary Tract Infection, has completed, sponsored by University of Washington.
- COMPLETED
- Registry status
- NA
- Development phase
- 300 participants
- Enrollment target
- 2
- Study locations
Study Summary
Urinary tract infection (UTI) is a very common problem in young healthy women, afflicting approximately one-half of women by their late 20s. One of the most common antibiotics used to treat UTIs is ciprofloxacin, usually for a total of three days. However, increasing resistance to this antibiotic has raised concerns about its overuse for cystitis and generated interest in alternative agents. An alternative antibiotic which is approved for use in UTIs is cefpodoxime. However, there are few studies evaluating the efficacy and tolerance of this compound when given in a 3-day regimen as is commonly used for treatment of UTI. The major purpose of this study is to assess the efficacy and tolerance of a 3-day regimen of cefpodoxime versus ciprofloxacin for treatment of acute uncomplicated cystitis.
Conditions Studied
Interventions
- DRUG Ciprofloxacin
- DRUG Cefpodoxime
Study Locations (2)
Florida
- University of Miami Miller School of Medicine - Miami
Washington
- University of Washington - Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2005-06 |
| Est. Completion | 2009-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00194532
The ClinicalTrials.gov registry entry for NCT00194532 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 646-participant average among 11 other Urinary Tract Infection trials with a reported enrollment target (54% lower). The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Urinary Tract Infection appearing as the primary indexed condition, and to 2 interventions - of which Ciprofloxacin is the first listed.
NCT00194532 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Florida, Washington.
Frequently Asked Questions
What is clinical trial NCT00194532 about?
NCT00194532 is a clinical study titled "Cefpodoxime vs Ciprofloxacin for Acute Cystitis". Urinary tract infection (UTI) is a very common problem in young healthy women, afflicting approximately one-half of women by their late 20s. One of the most common antibiotics used to treat UTIs is ciprofloxacin, usually for a total of three days. However, increasing resistance to this antibiotic ha...
What is the current status of trial NCT00194532?
This trial is currently completed. It is a NA study. The enrollment target is 300 participants. The study started on 2005-06. Estimated completion is 2009-02.
What conditions does trial NCT00194532 study?
This clinical trial studies the following conditions: Urinary Tract Infection.
What interventions are being tested in trial NCT00194532?
The interventions under investigation include: Ciprofloxacin (DRUG), Cefpodoxime (DRUG).
Who is sponsoring clinical trial NCT00194532?
This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00194532 being conducted?
This trial has 2 study locations across Florida, Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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