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Completed Phase 3 Interventional Results available

An Effectiveness and Safety Study for Levofloxacin in Chronic Prostatitis

ClinicalTrials.gov ID: NCT00402688

Public ClinicalTrials.gov record NCT00402688. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 12:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Double-Blind, Phase 3B Study to Compare the Safety and Clinical Efficacy of Levofloxacin in 750mg for 2 Weeks and Levofloxacin 750mg for 3 Weeks to That of Levofloxacin 500mg for 4 Weeks in the Treatment of Chronic Prostatitis

Study identification

NCT ID
NCT00402688
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Industry
Enrollment
242 participants

Conditions and interventions

Conditions

Interventions

  • levofloxacin Drug

Drug

Eligibility (public fields only)

Age range
40 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 31, 2006
Primary completion
Feb 29, 2008
Completion
Aug 31, 2008
Last update posted
Sep 12, 2013

2006 – 2008

United States locations

U.S. sites
39
U.S. states
21
U.S. cities
39
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Homewood Alabama
Not listed Anchorage Alaska
Not listed Hot Springs Arkansas
Not listed Fresno California
Not listed San Diego California
Not listed Denver Colorado
Not listed New Britain Connecticut
Not listed New Smyrna Beach Florida
Not listed Ocala Florida
Not listed Orlando Florida
Not listed Ormond Beach Florida
Not listed Plantation Florida
Not listed St. Petersburg Florida
Not listed Tallahassee Florida
Not listed Tampa Florida
Not listed Wellington Florida
Not listed Columbus Georgia
Not listed Roswell Georgia
Not listed Jeffersonville Indiana
Not listed Des Moines Iowa
Not listed Shreveport Louisiana
Not listed Greenbelt Maryland
Not listed St Louis Missouri
Not listed Las Vegas Nevada
Not listed Marlton New Jersey
Not listed Albuquerque New Mexico
Not listed Garden City New York
Not listed Kingston New York
Not listed New York New York
Not listed Orchard Park New York
Not listed Poughkeepsie New York
Not listed Staten Island New York
Not listed Salisbury North Carolina
Not listed Columbus Ohio
Not listed Bethany Oklahoma
Not listed Allentown Pennsylvania
Not listed Bala-Cynwyd Pennsylvania
Not listed State College Pennsylvania

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00402688, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 12, 2013 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00402688 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →