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Completed Phase 2 Interventional Results available

Study to Evaluate the Safety and Efficacy of Ciprofloxacin (Inhaled) in Patients With Cystic Fibrosis

ClinicalTrials.gov ID: NCT00645788

Public ClinicalTrials.gov record NCT00645788. 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 Sep 5, 2026, 5:27 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

Randomized, Double-blind, Placebo-controlled, Multicenter Study to Evaluate the Safety and Efficacy of Inhaled Ciprofloxacin Compared to Placebo in Subjects With Cystic Fibrosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the change in forced expiratory volume (FEV1) from baseline to Day 28-30 between Cipro Inhale-treated and placebo-treated subjects after a 4-week treatment period.

Study identification

NCT ID
NCT00645788
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bayer
Industry
Enrollment
288 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
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
Apr 30, 2008
Primary completion
Dec 31, 2010
Completion
Dec 31, 2010
Last update posted
Jun 8, 2014

2008 – 2011

United States locations

U.S. sites
58
U.S. states
28
U.S. cities
50
Facility City State ZIP Site status
Not listed Phoenix Arizona 85016
Not listed Tucson Arizona 85724
Not listed Little Rock Arkansas 72205
Not listed Los Angeles California 90027
Not listed Los Angeles California 90033
Not listed Los Angeles California 90048
Not listed Orange California 92868
Not listed San Diego California 92123-4282
Not listed San Francisco California 94143
Not listed Ventura California 93003
Not listed Aurora Colorado 80045
Not listed Hartford Connecticut 06102
Not listed New Haven Connecticut 06520
Not listed Jacksonville Florida 32207
Not listed Miami Florida 33136
Not listed Orlando Florida 32801
Not listed Orlando Florida 32803
Not listed Orlando Florida 32806
Not listed Augusta Georgia 30912-4005
Not listed Chicago Illinois 60612
Not listed Chicago Illinois 60614
Not listed Glenview Illinois 60025
Not listed Maywood Illinois 60153
Not listed Indianapolis Indiana 46202
Not listed Iowa City Iowa 52242-1089
Not listed Lexington Kentucky 40536-0284
Not listed Louisville Kentucky 40207
Not listed Boston Massachusetts 02111
Not listed Boston Massachusetts 02115
Not listed Ann Arbor Michigan 48109
Not listed Kalamazoo Michigan 49007
Not listed Jackson Mississippi 39216
Not listed Las Vegas Nevada 89107
Not listed Livingston New Jersey 07039
Not listed Long Branch New Jersey 07740
Not listed Morristown New Jersey 07962
Not listed Somerville New Jersey 08876
Not listed Albany New York 12208
Not listed New Hyde Park New York 11040
Not listed Valhalla New York 10595
Not listed Durham North Carolina 27710
Not listed Akron Ohio 44308-1062
Not listed Cincinnati Ohio 45229-3039
Not listed Toledo Ohio 43606
Not listed Oklahoma City Oklahoma 73104
Not listed Oklahoma City Oklahoma 73112
Not listed Tulsa Oklahoma 74145
Not listed Hershey Pennsylvania 17033-0850
Not listed Philadelphia Pennsylvania 19104-4283
Not listed Philadelphia Pennsylvania 19134
Not listed Charleston South Carolina 29425
Not listed Knoxville Tennessee 37916
Not listed Austin Texas 78723
Not listed San Antonio Texas 78212
Not listed Salt Lake City Utah 84132
Not listed Charlottesville Virginia 22908
Not listed Seattle Washington 98105
Not listed Madison Wisconsin 53792

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 28 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00645788, 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 Jun 8, 2014 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00645788 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →