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Completed Phase 4 Interventional

Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment of Subjects With Acute Bacterial Sinusitis

ClinicalTrials.gov ID: NCT00645073

Public ClinicalTrials.gov record NCT00645073. 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 21, 2026, 12:51 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 Phase IV Comparative Study of the Safety and Efficacy of Cefdinir and Levofloxacin for the Treatment of Subjects With Acute Bacterial Sinusitis

Study identification

NCT ID
NCT00645073
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Abbott
Industry
Enrollment
271 participants

Conditions and interventions

Interventions

  • cefdinir (Omnicef) Drug
  • levofloxacin Drug

Drug

Eligibility (public fields only)

Age range
18 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
Oct 31, 2003
Primary completion
Feb 29, 2004
Completion
Not listed
Last update posted
Mar 26, 2008

Started 2003

United States locations

U.S. sites
23
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
Not listed Birmingham Alabama 35211
Not listed Birmingham Alabama 35215
Not listed Columbiana Alabama 35051
Not listed Eclectic Alabama 36024
Not listed Tuscaloosa Alabama 35406
Not listed Mesa Arizona 85201
Not listed Fresno California 93703
Not listed Fresno California 93710
Not listed Murray Kentucky 42071
Not listed Portage Michigan 49024
Not listed Eugene Oregon 97404
Not listed Lake Oswego Oregon 97035
Not listed Orangeburg South Carolina 29118
Not listed Kingsport Tennessee 37660
Not listed Milan Tennessee 38358
Not listed Corsicana Texas 75110
Not listed San Antonio Texas 78205
Not listed Salt Lake City Utah 84109
Not listed Salt Lake City Utah 84121
Not listed West Jordan Utah 84084
Not listed West Jordan Utah 84088
Not listed Winchester Virginia 22601
Not listed Spokane Washington 99204

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00645073, 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 Mar 26, 2008 · Synced Jul 21, 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 NCT00645073 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →