Clinical Trials Directory

Trials / Completed

CompletedNCT01045902

BAY12-8039, iv/Oral Pulmonary Abscess/Aspiration Pneumonia

Prospective, Multi-center, Randomized, Non-blind Trial to Assess the Efficacy and Safety of Moxifloxacin Versus Sulbactam/Ampicillin in the Treatment of Pulmonary Abscess and Aspiration Pneumonia

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
139 (actual)
Sponsor
Bayer · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this trial is to determine the efficacy and safety of Moxifloxacin in comparison to Sulbactam/Ampicillin in the treatment of pulmonary abscesses and aspiration pneumonia.

Conditions

Interventions

TypeNameDescription
DRUGAvelox (Moxifloxacin, BAY12-8039)Moxifloxacin, 400 mg iv, od, switch after 6 doses (6 days) to 400 mg Moxifloxacin oral, od
DRUGSulbactam/AmpicillinSulbactam/Ampicillin, 3 g iv, tid, switch after 18 doses (6 days) to 750 mg Sulbactam/Ampicillin oral, bid

Timeline

Start date
2001-02-01
Completion
2005-01-01
First posted
2010-01-11
Last updated
2010-01-11

Locations

15 sites across 1 country: Germany

Source: ClinicalTrials.gov record NCT01045902. Inclusion in this directory is not an endorsement.