Clinical Trials Directory

Trials / Completed

CompletedNCT00879008

SYMPROVE III: Health Services Research Study for Treatment of the Moderate and Severe Acute Exacerbations of Chronic Bronchitis (AECB)

SYMPROVE III: Health Services Research Study for Treatment of the Moderate and Severe AECB

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

Summary

In this study data of patients with moderate or severe acute exacerbations of chronic bronchitis (AECB) were collected. There were two different cohorts which were compared (Moxifloxacin and other antibiotics) concerning effectiveness and tolerance. It was a prospective study which was accomplished in 100 ambulatory practice offices.

Detailed description

The study design was slightly changed to adapt the target population. Due to these changes the study was restarted on 8th December 2009.

Conditions

Interventions

TypeNameDescription
DRUGMoxifloxacin (Avelox, BAY12-8039)Patients from the normal praxis routine, treated with Moxifloxacin according to the local product information

Timeline

Start date
2009-12-01
Primary completion
2010-08-01
Completion
2010-08-01
First posted
2009-04-09
Last updated
2014-06-23

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00879008. Inclusion in this directory is not an endorsement.