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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
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00879008
Acronym
SYMPROVE III
Enrollment
345
Registered
2009-04-09
Start date
2009-12-31
Completion date
2010-08-31
Last updated
2014-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Bronchitis

Keywords

Disease Exacerbation, Acute Exacerbations of Chronic Bronchitis, AECB, Avelox, Bronchitis

Brief 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.

Interventions

Patients from the normal praxis routine, treated with Moxifloxacin according to the local product information

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Acute exacerbation of chronic bronchitis from Anthonisen type I or II * FEV1 of \< 50 % * Patient must be ensured in the statutory health insurance * Further contraindications of the prescribed pharmaceutical products must be considered

Exclusion criteria

* Patients who change from one cohort to the other

Design outcomes

Primary

MeasureTime frame
Effectiveness and tolerance of/to the different therapieswithin the first 14 days
Possible hospitalisation ratewithin the first 14 days

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026